chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
196541299865412999AAC12GENIChomozygous46189311
196541342865413429AG10GENIChomozygous46189312
196541358065413581AAC9GENIChomozygous46189313
196541425565414256CT21GENIChomozygous46189314
196541425865414259TC21GENIChomozygous46189315
196541475565414756GA11GENIChomozygous46189316
196541482165414822CT11GENIChomozygous46189317
196541694165416942GA7GENIChomozygous46189318
196541702265417023TTC7GENIChomozygous46189319
196541715465417168AAAAAAAAAAAAAA--------------9GENICpossibly homozygous46189320
196542298665422987CT18GENIChomozygous46189321
196542418265424183GA11GENIChomozygous46189322
196542421265424213CT14GENIChomozygous46189323
196542437365424374AG8GENIChomozygous46189324
196542692665426927TA12GENIChomozygous46189329
196542713965427140GGAA13GENICheterozygous46189330
196542726965427275TGGTGA------10GENIChomozygous46189331
196542741465427415CCA4GENIChomozygous46189332
196542875865428759CG8GENIChomozygous46189333
196543643065436431TC6GENIChomozygous46189340
196542713965427140GGAAA13GENICheterozygous46509156
196543110565431106CT4GENIChomozygous46189334
196543116765431168AG4GENIChomozygous46189335
196543287165432872TTC5GENIChomozygous46189337
196543627765436278TG14GENIChomozygous46189339
196543122565431226GGCTGCTGCTC4GENIChomozygous46383780
196543652065436521GGAA12GENICheterozygous46189341
196543652065436521GGA12GENICheterozygous46494831
196543656865436569AG7GENIChomozygous46189342
196543756265437563TC14GENIChomozygous46189343
196543876765438768GA19GENIChomozygous46189344
196543965865439659GA16GENIChomozygous46189345
196544076265440763AC7GENIChomozygous46189346