chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221504177221504179GT--1GENIChomozygous61094030
1221504555221504556GA28GENIChomozygous61094031
1221505977221505978CT25GENIChomozygous61094032
1221508190221508191CT23GENIChomozygous61094033
1221509246221509247CT19GENIChomozygous61094034
1221510285221510286TA19GENIChomozygous61094036
1221511993221511994AG19GENIChomozygous61094039
1221513366221513367TC12GENICpossibly homozygous61094040
1221514210221514211TC21GENICpossibly homozygous61094041
1221515199221515200AG11GENIChomozygous61094042
1221515517221515518CT6GENIChomozygous61094043