chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95257215752572158GA54GENIChomozygous507291877
95257223752572238TC69GENIChomozygous508569264
95257285452572855GT74GENIChomozygous507291878
95257290352572904AG73GENIChomozygous507291879
95257291752572918GT65GENICpossibly homozygous507291880
95257302652573027CCAGCACGA12GENIChomozygous686035616
95257311552573116CCA46GENIChomozygous686035617
95257321052573211CT62GENICpossibly homozygous508569265
95257419252574193AG54GENIChomozygous507291881
95257448952574490CT60GENIChomozygous507291882
95257469652574697TC52GENIChomozygous507291883
95257473752574738TC54GENIChomozygous507291884
95257489652574897GA64GENIChomozygous508569266
95257512052575121GA56GENIChomozygous507291885
95257545052575451AG90GENIChomozygous507291886
95257567052575671CT71GENIChomozygous508569267
95257567152575672AG72GENIChomozygous507291887
95257628052576281TG58GENIChomozygous507291888
95257632152576322GC61GENIChomozygous507291889
95257661052576611TC92GENIChomozygous507291890
95257665052576651TA67GENIChomozygous507291891
95257683152576832AG66GENIChomozygous507291892
95257701252577013AT74GENIChomozygous507291893
95257741352577414CT85GENICpossibly homozygous507291894
95257750252577503AT73GENIChomozygous507291895
95257762252577623AG66GENIChomozygous507291896
95257765652577657AG65GENIChomozygous507291897
95257811952578120CA38GENICpossibly homozygous508569268