chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133286970133286971AG41GENIChomozygous112832478
4133287184133287185TG43GENIChomozygous112832479
4133287420133287421AG54GENIChomozygous112832480
4133287634133287637ATT44GENIChomozygous128079965
4133288300133288301GC38GENIChomozygous112832481
4133288301133288302AT38GENIChomozygous112832482
4133288712133288713AG52GENIChomozygous112832483
4133290376133290377GC39GENIChomozygous112832485
4133290380133290381GC38GENIChomozygous112832486
4133291435133291435T41GENIChomozygous128079966
4133295704133295705GA50GENIChomozygous112832488
4133314814133314815GT23GENIChomozygous112832489
4133314824133314825CT26GENIChomozygous112832490
4133315669133315670AT1GENIChomozygous126023278
4133316675133316676GT37GENIChomozygous112832491
4133293609133293610A33GENICheterozygous131846400
4133293901133293902CA14GENICheterozygous128134118
4133316033133316034TC5GENIChomozygous128134119
4133316094133316095CT6GENIChomozygous128134120
4133316942133316942TTC52GENIChomozygous128079967
4133316950133316950ACTGACAT54GENIChomozygous128079968
4133317122133317123GC45GENIChomozygous112832492
4133317294133317295AG51GENIChomozygous112832493
4133318783133318784GA44GENIChomozygous112832494
4133320547133320548TC53GENIChomozygous112832495
4133320657133320658TA37GENIChomozygous112832496
4133322131133322145AAAAGGGTTTTGGC35GENIChomozygous128079969
4133322399133322400AG62GENIChomozygous112832497
4133322640133322641AG50GENIChomozygous112832498
4133323117133323119TT46GENIChomozygous128079970