chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1184184339184184340AATC13GENICheterozygous61313321
1184184349184184350CCTA8GENICheterozygous62272678
1184184353184184354CA9GENICheterozygous62872406
1184184618184184619GA20GENICheterozygous61567047
1184185799184185800GA10GENICheterozygous60998682
1184184394184184395CT13GENIChomozygous60998679
1184184740184184741CT17GENICheterozygous60998680
1184185044184185045GC15GENICheterozygous60998681
1184185916184185920TTTC----16GENICheterozygous61567048
1184185935184185936TC16GENIChomozygous60998683
1184185938184185939TC15GENICheterozygous60998684
1184186294184186295GA9GENIChomozygous60998686
1184186433184186434TC8GENIChomozygous60998689
1184187251184187252T-7GENIChomozygous61567051
1184188059184188060CT8GENIChomozygous60998692
1184188545184188546GGT13GENICheterozygous60998693
1184185839184185840TTACGATGG9GENICheterozygous62027522
1184188496184188497GA13GENICheterozygous62027523