chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2255895404255895405GA34GENIChomozygous111392291
2255895605255895606TA32GENIChomozygous110405158
2255896255255896256GT40GENIChomozygous111392293
2255896294255896295GA39GENIChomozygous111392295
2255896313255896314TG44GENIChomozygous111392297
2255897025255897026GT47GENIChomozygous110405160
2255897137255897138CA39GENIChomozygous110860965
2255898487255898488GA37GENIChomozygous111392299
2255898550255898551TC32GENIChomozygous111392301
2255899010255899011GA76GENICheterozygous111392303
2255900073255900074TC44GENIChomozygous110860971
2255900647255900648CT37GENICpossibly homozygous110405164
2255902687255902688GA41GENIChomozygous111392305
2255903027255903028TA55GENIChomozygous111392307
2255903350255903351TC47GENIChomozygous111041271
2255903531255903532GA54GENICpossibly homozygous111392309
2255904027255904028GA34GENIChomozygous110860981
2255904508255904509TC51GENIChomozygous111392311
2255904559255904560AG51GENIChomozygous110860985
2255904801255904802TC34GENIChomozygous111392313
2255905055255905056TC31GENIChomozygous110860987
2255905268255905269CT45GENIChomozygous111392315
2255905306255905307GA44GENIChomozygous111392316
2255905602255905603TC33GENIChomozygous111041284
2255905637255905638AG36GENIChomozygous111392318
2255905994255905995TG32GENIChomozygous110860991
2255906030255906031CG32GENIChomozygous111392320