chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221504177221504179GT--31GENIChomozygous61094030
1221504555221504556GA44GENIChomozygous61094031
1221505977221505978CT30GENIChomozygous61094032
1221508190221508191CT43GENIChomozygous61094033
1221509246221509247CT31GENIChomozygous61094034
1221509655221509656GA43GENICpossibly homozygous61094035
1221509690221509691GA46GENICheterozygous61321175
1221510285221510286TA45GENIChomozygous61094036
1221511361221511362CCGT10GENICheterozygous61094037
1221511361221511362CCGTGT10GENICheterozygous61094038
1221511993221511994AG36GENIChomozygous61094039
1221513366221513367TC31GENIChomozygous61094040
1221514210221514211TC27GENIChomozygous61094041
1221515199221515200AG31GENIChomozygous61094042
1221515517221515518CT50GENIChomozygous61094043
1221515714221515718CTTT----5GENICheterozygous61094044
1221515714221515717CTT---5GENICheterozygous61094045