chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------16GENIChomozygous731431015
85378107053781071CT27GENIChomozygous602020539
85378121053781211AG30GENICpossibly homozygous602020540
85378128753781288GGA11GENICheterozygous731431017
85378128753781288GGAAA11GENICheterozygous731431019
85378133353781334AG19GENIChomozygous602020541
85378146653781467AG30GENIChomozygous602020542
85378180553781806AG35GENIChomozygous602020543
85378193153781932TTTA18GENICheterozygous731431020
85378193153781932TTTTA18GENICheterozygous731431021
85378193153781932TTTTTA18GENICheterozygous731431022
85378200853782013GTTTG-----21GENIChomozygous731431023
85378241353782414CT35GENIChomozygous602020544
85378260753782608TC30GENIChomozygous602020545
85378277053782771GA27GENIChomozygous602020546
85378331953783320AG31GENIChomozygous602020547
85378340253783403T-19GENICpossibly homozygous731431024
85378373853783739GT35GENIChomozygous602020548
85378379353783794TC32GENIChomozygous602020549
85378391753783918T-14GENIChomozygous731431025
85378391953783926TGCGTGT-------14GENIChomozygous731431026
85378404853784049TC26GENIChomozygous602020550
85378550553785506T-16GENIChomozygous731431027
85378552153785522CCTTTT13GENIChomozygous731431029