chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
591772609177261GA45GENIChomozygous978912488
591775089177509GC46GENIChomozygous978912489
591775219177522TC50GENIChomozygous978912490
591777129177713TC41GENIChomozygous978912491
591779089177909TC17GENIChomozygous978912492
591784629178463GC11GENIChomozygous978912493
591789689178969CT23GENIChomozygous978912494
591792239179224GA14GENIChomozygous978912495
591792919179292TC27GENIChomozygous978912496
591795329179533GA23GENIChomozygous978912497
591797569179757GT22GENIChomozygous978912498
591798379179838CA18GENIChomozygous978912499
591807319180732GA31GENIChomozygous978912500
591810249181025TC31GENIChomozygous978912501