chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1217217861721787GA10GENIChomozygous139061479
1217217861721787G10GENICheterozygous403844900
1217217911721792CT10GENIChomozygous139061480
1217217921721793AG10GENIChomozygous139061481
1217221081722109TC18GENIChomozygous139061482
1217226351722636AG21GENIChomozygous139061483
1217226871722688GC18GENIChomozygous139061484
1217227481722749CA25GENIChomozygous139061485
1217229121722913CT16GENIChomozygous139061486
1217232731723274CT15GENIChomozygous139061487
1217234101723411TA11GENIChomozygous139061488
1217236031723604TG18GENIChomozygous139061489
1217239121723913TC27GENIChomozygous139061490
1217253031725304TC17GENIChomozygous139061491
1217258671725868CT20GENIChomozygous139061492
1217273321727333GT25GENICpossibly homozygous139061493
1217233371723338AC12GENIChomozygous154753818
1217228341722834T17GENIChomozygous139035731
1217218471721849CA25GENICpossibly homozygous145216736