chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138546559085465591AG66GENIChomozygous114422164
138546631885466319A46GENICpossibly homozygous129082548
138546684785466848GC51GENIChomozygous114422166
138546688385466884GA50GENIChomozygous114422168
138546737285467373GT61GENIChomozygous114422170
138546881685468817GA67GENIChomozygous114422172
138547254485472544TT44GENIChomozygous129082550
138547254585472546AT44GENIChomozygous114422174
138547349985473500TC48GENICpossibly homozygous114422176
138547423185474233GA14GENIChomozygous129082551
138547423685474238CA13GENIChomozygous129082552
138547424485474244A11GENIChomozygous129082553
138547424685474252AGCCCT10GENIChomozygous129082554
138547426385474264C12GENIChomozygous129082555
138547444185474441A36GENIChomozygous129082556
138547510785475108AG41GENIChomozygous114645884
138547091585470916AT46GENIChomozygous114830675
138547147385471485TTTCTTTCTTCT46GENIChomozygous133263451
138547252785472528TA49GENIChomozygous114645880
138547325885473259GA52GENIChomozygous114645882
138547529085475290T47GENIChomozygous129082557
138547538685475387AG54GENIChomozygous114422178
138547766385477664G51GENIChomozygous129082558
138547815885478158G46GENIChomozygous129082559
138547875785478758AG3GENIChomozygous126070408
138547636585476366TC66GENIChomozygous114422180
138547785685477857CT53GENIChomozygous114422182
138548021085480211CT7GENIChomozygous126070409
138548074685480747AG4GENIChomozygous123778420
138548354285483543TC3GENIChomozygous129113407
138548355785483558TC4GENIChomozygous118594194
138548363085483633TCC3GENIChomozygous129082560
138548370785483710TCC1GENIChomozygous129082561
138548374585483745C5GENIChomozygous129082562
138548797185487972TC8GENIChomozygous129113408
138548798685487987CT10GENIChomozygous129113409
138555279685552797TC8GENIChomozygous118464964
138548373185483732AC5GENIChomozygous114692323
138548572585485726CT2GENIChomozygous133270121
138555272085552721AG11GENIChomozygous133270122
138550076185500762GC3GENIChomozygous131926554