chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150685448150685449TC13GENIChomozygous975791363
5150685716150685717TC9GENIChomozygous975791364
5150686020150686021GA15GENIChomozygous975791365
5150686369150686370CT10GENIChomozygous975791366
5150686423150686424TC10GENIChomozygous975791367
5150686627150686628GA15GENIChomozygous975791368
5150687272150687273CT18GENIChomozygous975791369
5150687321150687322GA16GENICpossibly homozygous975791370
5150690906150690907TC14GENIChomozygous975791371
5150691762150691763GT13GENIChomozygous975791372
5150691895150691896CT9GENIChomozygous975791373
5150692007150692008GA7GENIChomozygous975791374
5150694736150694737TC7GENIChomozygous975791375
5150695315150695316CG17GENIChomozygous975791376
5150695753150695754GA17GENIChomozygous975791377
5150695760150695761CT17GENIChomozygous975791378
5150696514150696515CT10GENIChomozygous975791379
5150697024150697025CT12GENIChomozygous975791380
5150697094150697095CA10GENIChomozygous975791381
5150697095150697096AC11GENIChomozygous975791382
5150698126150698127CA16GENIChomozygous975791383
5150698211150698212GA12GENIChomozygous975791384
5150698221150698222CG11GENIChomozygous975791385
5150700013150700014GA19GENIChomozygous975791386
5150701466150701467TC32GENIChomozygous975791387
5150703071150703072AC6GENIChomozygous975791388