chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141084699141084700GT7GENIChomozygous56493997
5141085334141085335CT18GENIChomozygous56188115
5141085723141085724GA21GENIChomozygous56065265
5141085894141085895CT20GENIChomozygous55753855
5141085996141085998TG--10GENIChomozygous55907616
5141095401141095402AT21GENIChomozygous56235397
5141095659141095660CT18GENIChomozygous56235399
5141096194141096195TA11GENIChomozygous56235400
5141096280141096281CA20GENIChomozygous55753863
5141096316141096317AG19GENIChomozygous56235401
5141096926141096927CT22GENIChomozygous56235403
5141096941141096942GA23GENIChomozygous56235405
5141096968141096976CACACACG--------16GENIChomozygous56065270
5141099723141099724CT15GENIChomozygous56235406
5141099912141099913AG24GENIChomozygous55753870
5141101227141101228TC21GENIChomozygous55753874
5141102732141102736AAAA----14GENICpossibly homozygous56235408
5141103569141103570AG25GENIChomozygous55753876
5141103971141103972GA18GENIChomozygous55753878
5141104164141104165CT16GENIChomozygous56235409
5141104949141104955CTCTCT------8GENICheterozygous56493998
5141106674141106675GA24GENIChomozygous55907623
5141106720141106721GA17GENIChomozygous56235410
5141106819141106820TC11GENIChomozygous55753888
5141107460141107461CCAAAA14GENIChomozygous56457916
5141108056141108057TTAA8GENIChomozygous55907627
5141110763141110764TTTTATTATTATTATTA5GENIChomozygous56493999
5141110954141110955AC3GENIChomozygous56494000