chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91658104116581042C71GENIChomozygous131450948
91658108316581084AT59GENIChomozygous117674208
91658150816581509CA56GENIChomozygous117674210
91658152816581529GT60GENIChomozygous117674211
91658153316581534CA60GENIChomozygous117674213
91658288516582886AG49GENIChomozygous117674215
91658297916582980CT31GENIChomozygous117674217
91658313916583140T12GENIChomozygous131450949
91658346516583466AG4GENIChomozygous131458901
91658225316582254CT44GENIChomozygous117269552
91658319716583198GC14GENIChomozygous131458899
91658323516583236TC17GENIChomozygous131458900
91659798716597988GT11GENIChomozygous131897708
91660144616601447AT43GENIChomozygous117674227
91659831716598318TC62GENIChomozygous117674219
91659841116598412GA31GENIChomozygous117269554
91659860416598605CT12GENIChomozygous131704905
91659872316598724GC20GENIChomozygous131458902
91660046116600462AG55GENIChomozygous117674223
91660059516600596AT46GENIChomozygous117269557
91660115616601157TC51GENIChomozygous117674225
91660095916600960TC35GENICpossibly homozygous120362504
91660156316601567GAGT39GENIChomozygous131450952
91660186016601861AG49GENIChomozygous117269558
91660204316602043TGTCTGTGCTCGGTCATCTCACCATAGCCTGAGATCCATTGGCTC26GENIChomozygous131450953
91660293716602938CT47GENIChomozygous117674235
91660313716603138TC54GENIChomozygous117674237
91660347816603479T38GENICpossibly homozygous130772845
91660356516603565AACCCT30GENIChomozygous131450954
91660418216604188AAAAAC23GENIChomozygous131892616
91660485416604855GA6GENIChomozygous131704906
91660740316607404AG42GENIChomozygous117674239
91660767916607680AC57GENIChomozygous117674241
91660772316607724GT45GENIChomozygous117674243
91660794416607945TA53GENIChomozygous117269562
91660842416608425GA46GENIChomozygous117674245
91660860416608605GA48GENIChomozygous117674247
91660883616608837CA60GENIChomozygous117674249
91660984816609849GA53GENIChomozygous117674251