chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2206819039206819040CT14GENICpossibly homozygous59353577
2206819169206819170T-2GENICheterozygous59353579
2206820070206820071AG20GENIChomozygous59930542
2206820371206820372AG11GENIChomozygous59353584
2206820411206820412CT8GENIChomozygous59930543
2206820462206820463TA5GENIChomozygous62202253
2206820511206820512TG15GENICpossibly homozygous62202255
2206821785206821786CT19GENIChomozygous62202257
2206822007206822008AG24GENIChomozygous59353592
2206823375206823376TC24GENICpossibly homozygous60230874
2206824354206824355CT15GENICpossibly homozygous60230876
2206824671206824672CG7GENIChomozygous59353598
2206824885206824886GT25GENICpossibly homozygous59353600
2206820324206820325CG18GENIChomozygous60300950