chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1229173605229173606T-28GENICheterozygous61108420
1229173606229173607C-2GENIChomozygous61321865
1229174100229174101GC28GENIChomozygous61604406
1229174322229174323GGGAA39GENIChomozygous61108421
1229175406229175407CG32GENIChomozygous61108423
1229175800229175801GC48GENIChomozygous61604407
1229176659229176660AG32GENIChomozygous61108425
1229176692229176696TCTA----35GENIChomozygous61604408
1229178197229178198GC18GENIChomozygous61108426
1229178771229178772CA28GENIChomozygous61108429
1229178897229178898CA32GENIChomozygous61108430
1229179361229179362CT28GENIChomozygous61604409
1229179726229179727TC31GENIChomozygous61108431
1229180200229180201CT23GENIChomozygous61108434
1229180280229180281CT23GENIChomozygous61108437
1229180470229180471GA31GENIChomozygous61108438
1229182860229182861GT18GENIChomozygous61604410
1229176696229176697TG35GENICheterozygous61683265