chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165515768165515769CT11GENIChomozygous971656400
1165515901165515902AT18GENIChomozygous971656401
1165516316165516317GA15GENIChomozygous971656402
1165516385165516386TC27GENIChomozygous971656403
1165516956165516957GA38GENIChomozygous971656404
1165517271165517272GC28GENIChomozygous971656405
1165519823165519824TC24GENIChomozygous971656406
1165520851165520852GA20GENIChomozygous971656407
1165521025165521026CT26GENIChomozygous971656408
1165521576165521577GA36GENIChomozygous971656409
1165522002165522003CT25GENIChomozygous971656410
1165522405165522406CT13GENIChomozygous971656411
1165522406165522407CG13GENIChomozygous971656412
1165523734165523735GT29GENIChomozygous971656413
1165523762165523763CT27GENIChomozygous971656414
1165524310165524311TC12GENIChomozygous971656415
1165525629165525630TC25GENIChomozygous971656416
1165525770165525771TC41GENIChomozygous971656417
1165526964165526965TC28GENIChomozygous971656418
1165527324165527325CA17GENIChomozygous971656419
1165527481165527482AG24GENIChomozygous971656420
1165527942165527943CT19GENIChomozygous971656421
1165528020165528021CA29GENIChomozygous971656422
1165528136165528137AC21GENIChomozygous971656423
1165528448165528449CG24GENIChomozygous971656424
1165528468165528469TG28GENIChomozygous971656425
1165528554165528555TC28GENIChomozygous971656426
1165528709165528710CG11GENIChomozygous971656427
1165528792165528793AT13GENIChomozygous971656428
1165528959165528960AG20GENIChomozygous971656429
1165529106165529107GA22GENIChomozygous971656430
1165529198165529199CT30GENIChomozygous971656431
1165529466165529467TG9GENIChomozygous971656432