chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141084699141084700GT11GENIChomozygous56493997
5141085334141085335CT31GENIChomozygous56188115
5141085723141085724GA14GENIChomozygous56065265
5141085894141085895CT15GENIChomozygous55753855
5141085996141085998TG--9GENIChomozygous55907616
5141095401141095402AT22GENIChomozygous56235397
5141095659141095660CT15GENIChomozygous56235399
5141096194141096195TA16GENIChomozygous56235400
5141096280141096281CA18GENIChomozygous55753863
5141096316141096317AG13GENIChomozygous56235401
5141096926141096927CT16GENIChomozygous56235403
5141096941141096942GA14GENIChomozygous56235405
5141096968141096976CACACACG--------5GENIChomozygous56065270
5141099723141099724CT10GENIChomozygous56235406
5141099912141099913AG19GENIChomozygous55753870
5141101227141101228TC8GENIChomozygous55753874
5141102732141102736AAAA----10GENICpossibly homozygous56235408
5141103569141103570AG17GENIChomozygous55753876
5141103971141103972GA11GENIChomozygous55753878
5141104164141104165CT23GENIChomozygous56235409
5141104949141104955CTCTCT------5GENICheterozygous56493998
5141106674141106675GA13GENIChomozygous55907623
5141106720141106721GA12GENIChomozygous56235410
5141106819141106820TC19GENIChomozygous55753888
5141107460141107461CCAAAA4GENIChomozygous56457916
5141108056141108057TTAA8GENIChomozygous55907627
5141110954141110955AC4GENIChomozygous56494000