chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152064783152064784CT58GENIChomozygous55926578
5152065589152065593TGTG----1GENIChomozygous55798228
5152065667152065668GA8GENIChomozygous56291637
5152065764152065765G-3GENIChomozygous55798229
5152065764152065765GGT3GENIChomozygous55798230
5152065799152065803TGTG----2GENIChomozygous55798231
5152065839152065840AAC1GENIChomozygous55926580
5152065942152065946CTTA----6GENICheterozygous55798235
5152065958152065960AC--8GENICheterozygous55798237
5152065962152065963TTG7GENIChomozygous55798238
5152065963152065964GGT5GENICheterozygous55798239
5152066168152066170GT--8GENIChomozygous55798244
5152066195152066196TC19GENIChomozygous55798245
5152066252152066253TA9GENICheterozygous55926582
5152066263152066264AG10GENICpossibly homozygous55798247
5152066291152066292TC11GENIChomozygous55798248
5152066306152066307GC13GENICheterozygous55926584
5152066449152066450CCTG22GENIChomozygous55798249
5152067046152067047GA62GENIChomozygous55926588
5152067174152067175CT58GENICpossibly homozygous55926590
5152067773152067774AG33GENICpossibly homozygous55798254
5152067920152067921GA50GENIChomozygous55926592
5152068196152068197TC56GENIChomozygous55798259
5152068198152068199AC58GENICpossibly homozygous55798260
5152068923152068931ACACACAC--------3GENICheterozygous55798261
5152069458152069459GGAAA23GENIChomozygous55926594
5152069514152069515A-7GENICheterozygous55798262
5152071291152071292AG64GENIChomozygous55798265
5152071441152071442CT27GENICpossibly homozygous55926596
5152071539152071540AC42GENIChomozygous55798267
5152071892152071893CT45GENIChomozygous55926598
5152072371152072375GGAA----15GENIChomozygous55926600
5152073001152073002AG45GENIChomozygous55926602
5152073077152073078AG46GENIChomozygous55798268
5152073116152073117TC40GENIChomozygous55798269
5152073567152073568TC40GENIChomozygous55798271