chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171624046616240467CA37GENIChomozygous110969660
171624078116240782GA31GENIChomozygous110969662
171624231616242317GT43GENIChomozygous111173002
171624302916243030TC64GENICpossibly homozygous111398547
171624444316244444AG42GENIChomozygous110969664
171624464916244650CA24GENIChomozygous111173004
171624504416245045GA40GENIChomozygous110969666
171624517616245177TC22GENIChomozygous110969668
171624604616246047GA47GENICheterozygous111173006
171624633516246336GA31GENIChomozygous111173008
171624721416247215CT36GENIChomozygous111173010
171624751516247516TC31GENICheterozygous111173012
171624956416249565TC43GENIChomozygous110969678
171625326416253265GA36GENIChomozygous110969686
171624303516243036TC62GENICheterozygous119331809
171624598316245984TC71GENICheterozygous119268524
171624605416246055GA33GENICheterozygous111496232
171624861316248614GA41GENICpossibly homozygous111430512
171625444516254446GA42GENIChomozygous110969688
171625456516254566GA32GENIChomozygous111173014
171625614516256146TC41GENIChomozygous110969690
171625710916257110GA31GENIChomozygous110969692
171625728216257283AG24GENIChomozygous110969694
171625737316257374AG23GENIChomozygous110969696
171625805216258053GA31GENIChomozygous110969698
171625812416258125CT35GENIChomozygous110969700
171626004216260043GA24GENIChomozygous110969702
171626244616262447TC51GENIChomozygous110969704
171626331216263313GA56GENIChomozygous110969706
171626359116263592TC38GENIChomozygous110969708
171626551716265518AG29GENIChomozygous110969710
171626555616265557TC27GENIChomozygous110969712
171626652116266522AG45GENIChomozygous110969715
171626657316266574TC49GENIChomozygous110969717
171626812316268124GC43GENICheterozygous119357612
171626812616268127TC44GENICheterozygous119331812
171626824516268246GA29GENIChomozygous111173016
171626954416269545GA37GENIChomozygous110969725
171627250216272503AG49GENIChomozygous110969731