chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91658104116581042C21GENIChomozygous131450948
91658108316581084AT19GENIChomozygous117674208
91658150816581509CA36GENIChomozygous117674210
91658152816581529GT39GENIChomozygous117674211
91658153316581534CA39GENIChomozygous117674213
91658225316582254CT22GENIChomozygous117269552
91658288516582886AG18GENIChomozygous117674215
91658297916582980CT8GENIChomozygous117674217
91658313916583140T9GENIChomozygous131450949
91658319716583198GC4GENIChomozygous131458899
91658323516583236TC3GENIChomozygous131458900
91658346516583466AG2GENIChomozygous131458901
91659831716598318TC21GENIChomozygous117674219
91659841116598412GA12GENIChomozygous117269554
91659872316598724GC7GENIChomozygous131458902
91660046116600462AG26GENIChomozygous117674223
91660059516600596AT27GENIChomozygous117269557
91660115616601157TC29GENIChomozygous117674225
91660144616601447AT18GENIChomozygous117674227
91660156316601567GAGT21GENIChomozygous131450952
91660186016601861AG15GENIChomozygous117269558
91660204316602043TGTCTGTGCTCGGTCATCTCACCATAGCCTGAGATCCATTGGCTC11GENIChomozygous131450953
91660293716602938CT16GENIChomozygous117674235
91660313716603138TC17GENIChomozygous117674237
91660356516603565AACCCT9GENIChomozygous131450954
91660740316607404AG20GENIChomozygous117674239
91660767916607680AC29GENIChomozygous117674241
91660772316607724GT30GENIChomozygous117674243
91660794416607945TA14GENIChomozygous117269562
91660842416608425GA26GENIChomozygous117674245
91660860416608605GA27GENIChomozygous117674247
91660883616608837CA23GENIChomozygous117674249
91660984816609849GA34GENIChomozygous117674251
91659798716597988GT2GENIChomozygous131897708
91660485416604855GA5GENIChomozygous131704906
91660095916600960TC21GENICpossibly homozygous120362504
91660347816603479T10GENIChomozygous130772845