chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103856141638561419AGC---6GENIChomozygous768169882
103856179638561797CT14GENIChomozygous668526015
103856193738561938AG11GENICheterozygous668526016
103856233238562333AC5GENIChomozygous668526017
103856237438562375CG15GENICpossibly homozygous668526018
103856247838562479CA14GENIChomozygous668526019
103856272138562725GTGC----1GENIChomozygous768169883
103856282538562826TC10GENIChomozygous668526020
103856290738562908TTTTTA2GENIChomozygous768169884
103856298038562981TC11GENICpossibly homozygous668526021
103856307238563073CT4GENIChomozygous668526022
103856318138563182AG14GENICpossibly homozygous668526023
103856323638563237AC25GENICpossibly homozygous668526024
103856332638563327GA16GENIChomozygous668526025
103856365538563656CCAG13GENICheterozygous768169885
103856382938563830CT16GENICpossibly homozygous668526026
103856391038563912AA--3GENIChomozygous768169886
103856424338564244CG5GENIChomozygous668526027
103856438538564386AG2GENIChomozygous668526028
103856466438564665GA4GENIChomozygous668526029
103856470538564706TTC3GENIChomozygous768169887