chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41028029810280299CT29GENIChomozygous141598934
41028283010282831TA30GENIChomozygous141598935
41028357010283571TC27GENIChomozygous136969701
41028548010285481CT33GENIChomozygous141598936
41028568410285685AG20GENIChomozygous141598937
41028618710286188TC19GENIChomozygous141598938
41028678110286782AC28GENIChomozygous141598939
41028767210287673CT20GENIChomozygous141598940
41029049810290499CT27GENIChomozygous141598941
41029190910291910CT23GENIChomozygous141598942
41029540010295401TC21GENIChomozygous136969702
41029787710297878T17GENIChomozygous143045100
41029798610297991TTTTC11GENIChomozygous143045101
41029876710298768AG21GENIChomozygous141598943
41029939710299398CT16GENIChomozygous141598944
41029952810299529AC22GENIChomozygous141598945
41029952910299530CT22GENIChomozygous141598946
41030219310302197TATG20GENICheterozygous143045102
41030656410306565GA27GENIChomozygous141598947
41030818710308188GA16GENIChomozygous141598948
41030917510309175G21GENIChomozygous141574765
41029606010296061T10GENICheterozygous136866363
41029839110298391T23GENICpossibly homozygous141574761
41030148910301489T9GENIChomozygous141574762
41030150510301506T12GENIChomozygous141574763
41030218310302185TA16GENICheterozygous141574764
41030972410309724GTCTTACGT25GENIChomozygous141574766
41031238710312387TC24GENIChomozygous141574767
41031378110313782TG25GENIChomozygous141598949
41031416110314162GA22GENIChomozygous141598950
41031716910317170CG26GENIChomozygous141598951
41031897610318977CT16GENIChomozygous141598952
41031933210319332AGTC14GENIChomozygous141574768
41031939710319398GT11GENIChomozygous141598953
41031952410319525CT12GENIChomozygous141598954