chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154724607154724608TC48GENICpossibly homozygous60900716
1154724673154724674TC39GENICpossibly homozygous60900717
1154724879154724880CT44GENICheterozygous61766719
1154724903154724904GT51GENICheterozygous61766721
1154724904154724905CT53GENICheterozygous61766723
1154724935154724936AG64GENICheterozygous60900718
1154725020154725021CT58GENICheterozygous60900719
1154725036154725037TA54GENICheterozygous60900720
1154725069154725070TG43GENICheterozygous60900721
1154725076154725077TA43GENICheterozygous60900722
1154725203154725204GC33GENICpossibly homozygous60900723
1154725343154725344AG30GENIChomozygous60900724
1154725344154725345TC30GENIChomozygous60900725
1154725406154725407TG31GENIChomozygous60900727
1154725424154725425AC29GENIChomozygous60900729
1154725503154725504GC22GENIChomozygous60900730
1154725517154725518AG20GENIChomozygous60900731
1154725753154725754GC29GENIChomozygous61766725
1154725849154725850CA40GENIChomozygous61766727
1154725975154725976CT36GENIChomozygous60900733
1154726065154726066GT31GENIChomozygous61766729
1154726105154726106TC36GENIChomozygous60900736
1154726320154726321TA36GENIChomozygous61766731
1154726468154726469GA27GENICpossibly homozygous60900739
1154726573154726574CT26GENICpossibly homozygous61766733
1154726744154726745AG9GENIChomozygous61766735
1154726761154726762AT8GENIChomozygous61766737
1154726764154726765CT8GENIChomozygous61766739
1154726765154726766AG8GENIChomozygous61766740
1154726772154726773CT8GENIChomozygous61766742
1154726778154726779GA8GENIChomozygous61766744
1154726786154726787TG7GENIChomozygous61766746
1154726846154726847CT8GENICpossibly homozygous61766748
1154726847154726848CT8GENIChomozygous61766750
1154727155154727156GA25GENICpossibly homozygous61766751