chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125418777854187779GC13GENIChomozygous50260633
125418813754188138CT19GENIChomozygous50260635
125418889254188893AG3GENIChomozygous50547965
125418889554188896TTTTAGCTCAG2GENIChomozygous50547966
125418890054188901TTAGA3GENIChomozygous50547967
125418890554188906TTTGCCTAGCAA3GENIChomozygous50547968
125418895254188954AA--11GENICpossibly homozygous50260641
125418911654189117CCTTTT7GENIChomozygous50547969
125418947354189474CA24GENIChomozygous50260645
125419030154190302A-27GENIChomozygous50260647
125419041254190413CG19GENIChomozygous50260648
125419069254190693GGA35GENIChomozygous50260650
125419135854191359C-13GENICheterozygous50260654
125419190154191903TC--25GENICpossibly homozygous50260656
125419254554192546TTAA14GENICheterozygous50260658
125419254554192546TTAAA14GENICheterozygous50260660
125419267654192677TC27GENIChomozygous50260662
125419338854193389GA27GENIChomozygous50260664
125419364254193643CCT24GENICpossibly homozygous50260666
125419387454193875A-28GENICpossibly homozygous50260668
125419499254195040CTGCTTCAGGCTGCTGTGTACTAGCTGTCCTTGTGCCAGGCCCATCCC------------------------------------------------26GENIChomozygous50514493
125419562354195624CT18GENIChomozygous50260670
125419591454195915GA33GENIChomozygous50260672
125419621354196214GGAATA20GENIChomozygous50260674