chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185122578851225789AG8GENICpossibly homozygous46449693
185122609651226097TC22GENIChomozygous46759706
185122791151227912GT10GENIChomozygous46759707
185122798951227990CCTTG11GENIChomozygous46449709
185122830651228307TC9GENIChomozygous46759708
185122983651229837TC11GENIChomozygous46759709
185122998551229986TC7GENIChomozygous46759710
185123018151230182GA13GENIChomozygous46449712
185123098851230989CT23GENIChomozygous46759711
185123333751233338GC18GENIChomozygous46449715
185123459951234600GA8GENIChomozygous46759712
185123504451235045AG18GENICpossibly homozygous46449716
185123516351235164TC24GENICpossibly homozygous46759713
185123666751236668CA8GENIChomozygous46449717
185123784151237842TTATTC2GENIChomozygous46449721
185123840051238401TC11GENIChomozygous46449722
185124096151240962AG14GENICpossibly homozygous46449725
185124190851241909AG15GENICpossibly homozygous46449727
185124202551242026GA18GENIChomozygous46759715
185124220951242210AG18GENIChomozygous46759716
185124238851242389CT11GENICpossibly homozygous46759717
185124260851242609AC8GENIChomozygous46759718
185124313551243136TC13GENIChomozygous46759719
185124338951243390GT8GENICpossibly homozygous46759720
185123368851233689A-1GENIChomozygous46602965
185123527251235273CT6GENICheterozygous46854071