{"text_format":"3","workbook":"xls","n_sheets":6,"sheets":["blood_module_annotations_disease","caudate_1_module_annotations_disease","caudate_2_module_annotations_disease","blood_module_gene_ids","caudate_module_1_gene_ids","caudate_module_2_gene_ids"],"read":"whole","date_system":"1900","formulas":"cached_only"}

{"sheet":"blood_module_annotations_disease","index":0,"n_rows":20,"n_cols":1,"rows_kept":20,"flags":["formulas_cached_only"]}
["spinocerebellar ataxia 12"]
["spinocerebellar ataxia 8"]
["spinocerebellar ataxia type 2"]
["Bloom Syndrome"]
["spinocerebellar ataxia type 6 (disorder)"]
["spinocerebellar ataxia type 7"]
["machado-joseph disease"]
["spinocerebellar ataxia type 1"]
["spinocerebellar ataxia 10"]
["Werner Syndrome"]
["spinocerebellar ataxia 17"]
["Ataxia, Spinocerebellar"]
["cholesterol ester storage disease"]
["type 2 (disorder) pachyonychia congenita"]
["jadassohn lewandowsky type pachyonychia congenita"]
["spinocerebellar ataxia 14"]
["Wolman Disease"]
["Diastrophic dysplasia"]
["spinocerebellar degeneration"]
["Hypogonadotropic hypogonadism"]

{"sheet":"caudate_1_module_annotations_disease","index":1,"n_rows":20,"n_cols":1,"rows_kept":20,"flags":["formulas_cached_only"]}
["neu-laxova syndrome"]
["Rieger syndrome"]
["paroxysmal kinesigenic choreoathetosis"]
["spinocerebellar ataxia type 1"]
["Ataxia, Spinocerebellar"]
["spinocerebellar ataxia type 6 (disorder)"]
["spinocerebellar ataxia 12"]
["machado-joseph disease"]
["spinocerebellar ataxia type 2"]
["spinocerebellar ataxia type 7"]
["spinocerebellar ataxia 8"]
["spinocerebellar ataxia 10"]
["spinocerebellar ataxia 17"]
["type i primary hyperoxaluria"]
["tuberous sclerosis 2 (disorder)"]
["niemann-pick disease, type c"]
["type 2 (disorder) pachyonychia congenita"]
["hereditary gingival fibromatosis"]
["ancell-spiegler cylindromas"]
["Noonan Syndrome"]

{"sheet":"caudate_2_module_annotations_disease","index":2,"n_rows":20,"n_cols":1,"rows_kept":20,"flags":["formulas_cached_only"]}
["spinocerebellar ataxia 10"]
["spinocerebellar ataxia type 7"]
["opitz-frias syndrome"]
["spinocerebellar ataxia 12"]
["spinocerebellar ataxia 8"]
["Ataxia, Spinocerebellar"]
["spinocerebellar ataxia type 1"]
["machado-joseph disease"]
["wieacker-wolff syndrome"]
["Rieger syndrome"]
["spinocerebellar ataxia 17"]
["spinocerebellar ataxia type 2"]
["spinocerebellar ataxia type 6 (disorder)"]
["fukuyama type congenital muscular dystrophy"]
["congenital muscular dystrophy (disorder)"]
["turcot syndrome (disorder)"]
["paroxysmal kinesigenic choreoathetosis"]
["alpha-Dystroglycanopathies"]
["spinocerebellar degeneration"]
["rubinstein-taybi syndrome"]

{"sheet":"blood_module_gene_ids","index":3,"n_rows":46,"n_cols":1,"rows_kept":46,"flags":["formulas_cached_only"]}
["ENSG00000129474"]
["ENSG00000002587"]
["ENSG00000116014"]
["ENSG00000104883"]
["ENSG00000175582"]
["ENSG00000114107"]
["ENSG00000149179"]
["ENSG00000124920"]
["ENSG00000171444"]
["ENSG00000162004"]
["ENSG00000197299"]
["ENSG00000186648"]
["ENSG00000105974"]
["ENSG00000001460"]
["ENSG00000120903"]
["ENSG00000176273"]
["ENSG00000215105"]
["ENSG00000070087"]
["ENSG00000232022"]
["ENSG00000115257"]
["ENSG00000229982"]
["ENSG00000178078"]
["ENSG00000205581"]
["ENSG00000071539"]
["ENSG00000152217"]
["ENSG00000106366"]
["ENSG00000168350"]
["ENSG00000224023"]
["ENSG00000183208"]
["ENSG00000181039"]
["ENSG00000160752"]
["ENSG00000256812"]
["ENSG00000170835"]
["ENSG00000170356"]
["ENSG00000135643"]
["ENSG00000135763"]
["ENSG00000201221"]
["ENSG00000145911"]
["ENSG00000114529"]
["ENSG00000181019"]
["ENSG00000131016"]
["ENSG00000188011"]
["ENSG00000156475"]
["ENSG00000198464"]
["ENSG00000197465"]
["ENSG00000140104"]

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