chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91658108316581084AT19GENIChomozygous117681454
91658150816581509CA31GENIChomozygous117674210
91658152816581529GT30GENIChomozygous117674211
91658153316581534CA30GENIChomozygous117681456
91658225316582254CT19GENIChomozygous117269552
91660046116600462AG21GENIChomozygous117681458
91660059516600596AT22GENIChomozygous117269557
91660095916600960TC19GENIChomozygous120362504
91660115616601157TC27GENIChomozygous117681462
91660186016601861AG23GENIChomozygous117269558
91660293716602938CT35GENIChomozygous117681464
91660313716603138TC34GENIChomozygous117681466
91660356416603565CT6GENIChomozygous117792161
91660767916607680AC27GENIChomozygous117681468
91660772316607724GT29GENICpossibly homozygous117681470
91660794416607945TA39GENIChomozygous117269562
91660842416608425GA19GENIChomozygous117681472
91660860416608605GA26GENIChomozygous117681474
91660883616608837CA25GENIChomozygous117681476
91660984816609849GA32GENIChomozygous117681478