chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
39120660191206601AA51GENIChomozygous134193264
39120669991206700AT54GENIChomozygous111653557
39120671091206711TA54GENIChomozygous111653558
39120785491207855AG52GENIChomozygous111653560
39120788891207889TG62GENIChomozygous111653561
39120821191208212GA46GENIChomozygous111653562
39120827491208275TC53GENIChomozygous111653563
39120836691208367TC57GENIChomozygous111653564
39120902691209027AC53GENICpossibly homozygous111653566
39120955791209558AG66GENIChomozygous111653568
39120995091209951CT77GENIChomozygous111653569
39121014891210149CT59GENIChomozygous111653570
39121094391210944TG49GENIChomozygous111653571
39121131091211311AG61GENIChomozygous111653572
39121182491211825GC62GENIChomozygous111653573
39121341891213419CT48GENIChomozygous111653577
39121532191215322TC56GENIChomozygous112253769
39121145691211457GA59GENIChomozygous112253767
39121180791211808GA58GENIChomozygous112253768
39120838491208384A53GENIChomozygous127908458
39120962191209621G62GENIChomozygous127908459