chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1167044564167044565AC5GENIChomozygous108955406
1167048129167048130GA14GENIChomozygous108357449
1167053632167053633CT11GENIChomozygous109522795
1167054712167054713CT4GENIChomozygous108955413
1167057618167057619CA15GENIChomozygous108357456
1167059074167059075CT13GENIChomozygous108955415
1167059858167059859GC5GENIChomozygous108357459
1167054514167054515GA7GENIChomozygous120487425
1167056551167056552AT14GENIChomozygous120487426
1167056786167056787CG12GENIChomozygous109164232
1167062240167062241GA6GENIChomozygous108955417
1167063773167063774TC9GENIChomozygous108955418
1167065299167065300CT17GENIChomozygous108955419
1167067061167067062TC8GENIChomozygous108357467
1167067282167067283AG15GENIChomozygous108357468
1167067790167067791GT16GENIChomozygous108357469
1167068981167068982GA16GENIChomozygous109522796
1167070355167070356CT13GENIChomozygous108955421
1167070919167070920AG10GENIChomozygous108357474
1167071006167071007AG13GENIChomozygous108357475
1167071617167071618CT8GENIChomozygous109522797
1167071892167071893CT11GENIChomozygous108955422
1167075621167075622TG6GENIChomozygous108357476
1167077342167077343CT18GENIChomozygous108955423
1167078881167078882CG8GENIChomozygous108357479
1167079228167079229TA12GENIChomozygous108357480
1167079391167079392CT13GENIChomozygous109522798
1167079736167079737TC8GENIChomozygous108357481
1167083192167083193AG11GENIChomozygous108357485
1167083380167083381TC13GENIChomozygous108357486
1167084006167084007AG12GENIChomozygous108357487
1167084062167084063AG16GENIChomozygous108357488
1167084179167084180TC17GENIChomozygous108955424
1167084643167084644AG14GENIChomozygous108357490
1167085022167085023TC16GENIChomozygous108357492
1167085033167085034GA11GENIChomozygous108357493
1167085928167085929GA11GENIChomozygous109522799
1167087375167087376CT9GENIChomozygous108357495
1167091285167091286TA9GENIChomozygous109522800
1167091299167091300TC7GENIChomozygous108357497