chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91658108316581084AT18GENIChomozygous117681454
91658150816581509CA26GENIChomozygous117674210
91658152816581529GT27GENIChomozygous117674211
91658153316581534CA27GENIChomozygous117681456
91658225316582254CT26GENIChomozygous117269552
91658288516582886AG27GENIChomozygous117674215
91658297916582980CT15GENIChomozygous117674217
91659831716598318TC25GENIChomozygous117674219
91659841116598412GA12GENIChomozygous117269554
91660035016600351GA16GENICheterozygous117674221
91660046116600462AG26GENIChomozygous117681458
91660059516600596AT31GENIChomozygous117269557
91660115616601157TC22GENIChomozygous117681462
91660144616601447AT25GENIChomozygous117674227
91660186016601861AG24GENIChomozygous117269558
91660200816602009TG30GENICheterozygous117674229
91660203716602038CT31GENICheterozygous117674231
91660204216602043TC31GENICheterozygous117674233
91660293716602938CT18GENIChomozygous117681464
91660313716603138TC25GENIChomozygous117681466
91660740316607404AG28GENIChomozygous117674239
91660767916607680AC19GENIChomozygous117681468
91660772316607724GT19GENIChomozygous117681470
91660794416607945TA23GENIChomozygous117269562
91660842416608425GA27GENIChomozygous117681472
91660860416608605GA16GENIChomozygous117681474
91660883616608837CA26GENIChomozygous117681476
91660984816609849GA18GENIChomozygous117681478