chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48034373480343735CT80GENIChomozygous112744957
48034726580347266CT48GENIChomozygous112744959
48034869680348697GT48GENIChomozygous112744961
48034957780349578TC85GENIChomozygous112744963
48035054380350544GA49GENIChomozygous112744965
48035083580350836TA33GENICheterozygous112744971
48035155080351551CT58GENIChomozygous112744973
48035181580351816AG49GENIChomozygous112744975
48035238080352381AG75GENICpossibly homozygous112744977
48035268280352683AT63GENIChomozygous112744980
48035280680352807TC59GENIChomozygous112744982
48035523080355231TG54GENIChomozygous112744984
48035637680356377AG41GENIChomozygous112744986
48035687980356880CT50GENIChomozygous112744988
48035751880357519TC62GENIChomozygous112744990
48035781080357811TA71GENIChomozygous112744992
48035954480359545CA67GENIChomozygous112744994
48035982580359826GT53GENIChomozygous112744996
48036050180360502TG67GENIChomozygous112744998
48036061880360619TG70GENIChomozygous112745000
48036099580360996CT80GENIChomozygous112745002
48036134480361345TC73GENIChomozygous112745004
48036331180363312CG71GENICpossibly homozygous112745006
48036522680365227CT59GENIChomozygous112745008
48036559780365598CA64GENIChomozygous112745010
48036609980366100CT62GENIChomozygous112745012
48036671680366717AC75GENICpossibly homozygous112745014