chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139037978790379788AG16GENIChomozygous114574392
139038030790380309CG21GENIChomozygous131134223
139038311890383119TC14GENIChomozygous114574394
139038334590383351CACGCA8GENIChomozygous131134224
139038338290383448ACACATGCACACACACGCACACACACACACACATGCACGCACACGCACGCGCACACGCACGCGCAT2GENIChomozygous131134225
139038346690383467TG1GENIChomozygous118536788
139038347990383537CACACGCACATGCACGCACACGCACACACACACGCACACACACATGCACACACATGCG1GENIChomozygous131134226
139038385190383853CA10GENIChomozygous131134227
139038566190385662CT15GENIChomozygous114574396
139038803190388032TC9GENIChomozygous114574398
139038868590388686TA12GENIChomozygous114574400
139038869890388699GA13GENIChomozygous114574402
139038876690388767GA16GENIChomozygous114574404
139038906590389066GA17GENIChomozygous114574406
139039073290390733AG15GENIChomozygous114574408
139039102490391025AG11GENIChomozygous114574409
139039200690392007C11GENICheterozygous131134228
139039252690392527A10GENIChomozygous131134229
139039730290397303TC13GENIChomozygous114574411
139039757590397576TC7GENIChomozygous114574413
139039775790397758AG17GENIChomozygous114574415
139040038590400386T10GENIChomozygous131134230
139040164390401644AG16GENIChomozygous114574417
139040194190401942GA28GENIChomozygous114574419
139040242490402425TG17GENIChomozygous114574421
139040298890402988C19GENIChomozygous131134231
139040298990402990GA20GENIChomozygous114574423
139040471790404718AT7GENIChomozygous114574425