chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149371534149371535TC36GENIChomozygous113242790
4149373313149373314GA29GENIChomozygous112881399
4149373336149373337TC35GENIChomozygous112881401
4149375226149375227AG18GENIChomozygous119413066
4149375417149375418AG28GENIChomozygous112881407
4149378911149378912GA26GENIChomozygous113242794
4149379844149379845TC27GENIChomozygous112881414
4149379951149379952AG26GENIChomozygous112881415
4149380209149380210GA21GENIChomozygous112881416
4149380449149380450TC25GENIChomozygous112881417
4149380612149380613CG31GENIChomozygous112881419
4149380734149380735TC18GENIChomozygous112881420
4149381039149381040CT30GENIChomozygous112881421
4149381041149381042GT28GENIChomozygous112881422
4149381043149381044GC28GENIChomozygous112881423
4149381157149381158CG24GENIChomozygous119587884
4149382257149382258TG24GENIChomozygous112881425
4149383073149383074CT26GENIChomozygous112881428
4149383279149383280GC30GENIChomozygous112881429
4149384051149384052CT25GENIChomozygous112881430
4149385585149385586CT25GENIChomozygous112881433
4149385925149385926AG31GENIChomozygous112881434
4149385983149385984GA22GENIChomozygous112881435
4149386002149386003CG23GENIChomozygous112881436
4149386088149386089AG26GENIChomozygous112881437
4149386795149386796AG21GENIChomozygous112881438
4149387147149387148TG27GENICpossibly homozygous119413067
4149387420149387421TA24GENIChomozygous112881439
4149389245149389246AT20GENIChomozygous112881441
4149389514149389515TC34GENIChomozygous112881442
4149392081149392082GA39GENIChomozygous112881445
4149392107149392108AT30GENIChomozygous112881446
4149392254149392255AG22GENIChomozygous119413068
4149395432149395433TC29GENIChomozygous112881447