chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8123734573123734574GA45GENIChomozygous138441220
8123735037123735038GA39GENIChomozygous142107903
8123735050123735051TA38GENIChomozygous142107904
8123735391123735392AG28GENIChomozygous142107905
8123735698123735699TG43GENIChomozygous142107906
8123736562123736563GT62GENIChomozygous138441222
8123736612123736613CT60GENIChomozygous138441223
8123737067123737068CT77GENICpossibly homozygous142107907
8123737411123737412GA62GENIChomozygous138441226
8123737501123737502CA55GENIChomozygous142107908
8123737751123737752AG56GENIChomozygous142107909
8123738850123738851CT51GENIChomozygous142107910
8123739556123739557TC28GENIChomozygous142107911
8123739687123739688CT62GENIChomozygous142107912
8123740089123740090GA50GENIChomozygous138441229
8123740276123740277CT57GENIChomozygous142107913
8123736134123736134GGAATGT41GENIChomozygous142032351
8123740958123740958T60GENIChomozygous142032352