chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1210976816210976817GC29GENIChomozygous61074508
1210977080210977081CT33GENICpossibly homozygous61074509
1210982639210982640TC26GENICpossibly homozygous61074510
1210982657210982658C-25GENIChomozygous61074511
1210982657210982658CCACA13GENIChomozygous61074512
1210982667210982668A-21GENIChomozygous61074513
1210982667210982668AAC20GENICheterozygous61074514
1210982685210982686CT32GENICheterozygous61074515
1210982687210982688CT32GENICheterozygous61318764
1210986448210986449AG27GENIChomozygous61074516
1210986661210986665TGTG----13GENICheterozygous61074517
1210986906210986907CT29GENIChomozygous61074518
1210989767210989768TTCACACA3GENIChomozygous61074520
1210991609210991610GA23GENIChomozygous61074521
1210991921210991922GA30GENIChomozygous61074522