chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221504177221504179GT--41GENIChomozygous61094030
1221504555221504556GA39GENIChomozygous61094031
1221505977221505978CT56GENIChomozygous61094032
1221508190221508191CT47GENIChomozygous61094033
1221509246221509247CT29GENIChomozygous61094034
1221509655221509656GA29GENICheterozygous61094035
1221510285221510286TA37GENIChomozygous61094036
1221511361221511362CCGT26GENICheterozygous61094037
1221511361221511362CCGTGT26GENICheterozygous61094038
1221511993221511994AG59GENIChomozygous61094039
1221513366221513367TC55GENIChomozygous61094040
1221514210221514211TC49GENIChomozygous61094041
1221515199221515200AG36GENIChomozygous61094042
1221515517221515518CT32GENIChomozygous61094043
1221515714221515718CTTT----6GENICheterozygous61094044
1221515714221515717CTT---6GENICheterozygous61094045