chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41028029810280299CT22GENIChomozygous141598934
41028283010282831TA33GENIChomozygous141598935
41028548010285481CT29GENIChomozygous141598936
41028568410285685AG29GENIChomozygous141598937
41028618710286188TC16GENIChomozygous141598938
41028678110286782AC28GENIChomozygous141598939
41028767210287673CT27GENIChomozygous141598940
41029049810290499CT25GENIChomozygous141598941
41029190910291910CT20GENIChomozygous141598942
41029876710298768AG23GENIChomozygous141598943
41029939710299398CT22GENIChomozygous141598944
41029952810299529AC29GENIChomozygous141598945
41029952910299530CT28GENIChomozygous141598946
41028357010283571TC31GENIChomozygous136969701
41029540010295401TC26GENIChomozygous136969702
41029606010296061T7GENIChomozygous136866363
41029787710297878T12GENIChomozygous143045100
41029798610297991TTTTC7GENIChomozygous143045101
41029839110298391T15GENIChomozygous141574761
41030148910301489T15GENICpossibly homozygous141574762
41030150510301506T14GENIChomozygous141574763
41030218310302185TA19GENIChomozygous141574764
41030656410306565GA23GENIChomozygous141598947
41030818710308188GA18GENIChomozygous141598948
41030917510309175G19GENIChomozygous141574765
41030972410309724GTCTTACGT25GENIChomozygous141574766
41031238710312387TC30GENIChomozygous141574767
41031378110313782TG22GENIChomozygous141598949
41031416110314162GA19GENIChomozygous141598950
41031716910317170CG27GENIChomozygous141598951
41031897610318977CT15GENIChomozygous141598952
41031933210319332AGTC18GENIChomozygous141574768
41031939710319398GT20GENIChomozygous141598953
41031952410319525CT20GENIChomozygous141598954