chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187611057187611062TTTTC5GENIChomozygous131297892
2187611092187611093GT8GENIChomozygous110167563
2187611815187611816CT21GENIChomozygous110167564
2187612300187612301AG29GENIChomozygous110167566
2187613004187613005GA20GENIChomozygous111343834
2187614464187614465AG23GENIChomozygous110167567
2187614973187614974GA16GENIChomozygous111343836
2187615132187615133GT13GENIChomozygous111343838
2187616518187616519TC16GENICpossibly homozygous110167569
2187618414187618415AT16GENIChomozygous110167570
2187619054187619054GTTT16GENIChomozygous127716968
2187621037187621038TC13GENIChomozygous110167571
2187621410187621411CT13GENIChomozygous111343840
2187621716187621717G11GENIChomozygous127716969
2187621956187621957CT16GENIChomozygous110167573
2187622246187622247AC18GENIChomozygous110167574