chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47655815876558159GA50GENIChomozygous137095857
47656112476561128TACT60GENIChomozygous136893886
47656347576563476GA33GENIChomozygous141634091
47656406076564061TC50GENIChomozygous137095859
47656406176564062TC49GENIChomozygous137095860
47656806976568070AG57GENIChomozygous137095863
47658017976580179G42GENIChomozygous136893892
47656530776565317CTGGCAATAG61GENIChomozygous146090480
47657076376570764GT43GENICheterozygous154188235
47657076476570765GT43GENICpossibly homozygous154188236
47656927076569271CT60GENIChomozygous146108346
47656994876569949TC64GENIChomozygous146108347
47657076376570764G43GENICpossibly homozygous403104204
47657076476570765G43GENICheterozygous403104205
47658532476585325TC66GENIChomozygous137095873
47658723676587238TA34GENIChomozygous136893893
47659289476592895GA44GENIChomozygous146108348
47659534476595345GA51GENIChomozygous137095880
47659705776597058TC44GENIChomozygous141634094
47660270476602704AGTTAGAATCCTATCACTGACCGTGTCTC67GENIChomozygous136893895
47661100776611008GT61GENIChomozygous146108349
47661241076612411TG50GENIChomozygous137095892
47661456276614563G71GENIChomozygous146090482
47661456676614567GT72GENIChomozygous146108350
47661602076616020G59GENIChomozygous146090483
47661602176616021GAA61GENIChomozygous146090484
47661942176619422AG73GENIChomozygous137095894
47662038576620386GA61GENIChomozygous146108351
47662506076625061CA79GENIChomozygous146108352
47662543976625440GA62GENIChomozygous146108353
47659100776591007T54GENICpossibly homozygous141582109
47660343976603439T39GENIChomozygous141582110