chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103595734235957343GA31GENIChomozygous116758264
103596005535960056TG23GENIChomozygous116559340
103596194535961946CG16GENIChomozygous116559346
103596252835962529TC26GENIChomozygous116559348
103596255135962552GA24GENIChomozygous116559350
103596257735962578AG26GENIChomozygous116559352
103596262435962625CT20GENIChomozygous116559354
103596263635962637GA21GENIChomozygous116559356
103596264835962649TC20GENIChomozygous116559358
103596265635962657GA26GENIChomozygous116559360
103596266335962664AG24GENIChomozygous116559362
103596302435963025TC24GENIChomozygous116559364
103596320435963205TC24GENICpossibly homozygous116559366
103596326635963267CT34GENIChomozygous116758266
103596333935963340TA28GENIChomozygous116559368
103596345435963455TA28GENIChomozygous116559370
103596369735963698CT26GENIChomozygous116758268
103596400235964003AG19GENIChomozygous116758270
103596401035964011TA16GENIChomozygous116924914
103596411835964119TG15GENIChomozygous116758272
103596420635964207GA22GENIChomozygous116758274
103596452135964522GT24GENIChomozygous116758276