chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157613725157613726GA18GENIChomozygous960826544
4157613853157613854GT24GENIChomozygous960826545
4157614185157614186TG21GENIChomozygous960826546
4157614774157614775AT26GENIChomozygous960826547
4157614977157614978AC18GENIChomozygous960826548
4157616535157616536CA16GENIChomozygous960826549
4157619978157619979GT23GENIChomozygous960826550
4157620744157620745TC31GENIChomozygous960826551
4157621147157621148CT14GENIChomozygous960826552
4157623083157623084GA31GENIChomozygous960826553
4157625710157625711CT18GENIChomozygous960826554
4157626447157626448TC35GENIChomozygous960826555
4157627043157627044TC27GENIChomozygous960826556
4157629525157629526TC31GENIChomozygous960826557
4157630918157630919GT16GENIChomozygous960826558
4157631950157631951AG26GENIChomozygous960826559
4157632657157632658TC22GENIChomozygous960826560
4157634098157634099TC27GENIChomozygous960826561
4157635239157635240AC22GENIChomozygous960826562
4157635295157635296CT20GENIChomozygous960826563
4157639657157639658GC28GENIChomozygous960826564
4157644216157644217CG22GENIChomozygous960826565
4157644340157644341TC24GENIChomozygous960826566