chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1276495458276495459GA13GENIChomozygous61230571
1276500264276500265TA11GENICpossibly homozygous61230572
1276500652276500653CT17GENICpossibly homozygous61230573
1276502551276502552AT12GENICpossibly homozygous61230574
1276502943276502944AG23GENICpossibly homozygous61230575
1276506189276506190GA23GENIChomozygous61230576
1276506563276506565AA--2GENICheterozygous62112909
1276506565276506566AACTT2GENICheterozygous62112910
1276506650276506651GGT2GENIChomozygous61230578
1276506721276506722AC8GENIChomozygous61230579
1276506797276506798GC25GENICpossibly homozygous61230580
1276506910276506911GA16GENIChomozygous61230581
1276507404276507405TG12GENIChomozygous61230582
1276508042276508043T-13GENIChomozygous61230583
1276509192276509193GA4GENIChomozygous61230584
1276509201276509202TTTA1GENIChomozygous61230585
1276509322276509326TTTG----10GENIChomozygous61230586
1276509419276509420TC17GENICheterozygous62218692
1276509420276509421CT17GENICheterozygous61820720
1276509769276509770CT6GENIChomozygous61230587
1276510070276510071GA9GENIChomozygous61230588
1276511425276511426AT5GENIChomozygous61230589
1276511538276511539GA11GENICheterozygous61230590
1276512095276512096TC11GENIChomozygous61230591
1276522037276522038GT8GENICheterozygous61230593
1276525756276525757AT12GENIChomozygous61230595
1276527370276527371AG13GENIChomozygous61230598