chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149413648149413649GA20GENIChomozygous652096597
4149413834149413835TG20GENIChomozygous652096598
4149414184149414185TC12GENIChomozygous652096599
4149415196149415197CT21GENIChomozygous652096600
4149415245149415246T-14GENIChomozygous758299091
4149415868149415869AG19GENIChomozygous652096601
4149415940149415945AAAGG-----11GENIChomozygous758299092
4149415964149415965GGT8GENICheterozygous758299093
4149416020149416021TC19GENIChomozygous652096602
4149416561149416562TTAGAAAGGCTTTAAGCTTTCATAATCCAGAGGTCTGAAACAATTATGTGCTAGAA6GENIChomozygous758299094
4149417979149417981GG--11GENICheterozygous758299095
4149417980149417981G-11GENICheterozygous758299096
4149418788149418789AG12GENIChomozygous652096603
4149419103149419104GA24GENIChomozygous652096604
4149420080149420081T-3GENICheterozygous758299097
4149420199149420200GA16GENIChomozygous652096605
4149420394149420395C-7GENIChomozygous758299098
4149420398149420419AACAAAAAACAAAAAAAAACC---------------------6GENICheterozygous758299099
4149420399149420419ACAAAAAACAAAAAAAAACC--------------------6GENICheterozygous758299100
4149420584149420585CCT21GENIChomozygous758299101
4149421568149421569TTAA8GENICheterozygous758299104
4149421569149421572AAA---8GENICpossibly homozygous758299102
4149421912149421913TG17GENIChomozygous652096606
4149422042149422043CT16GENIChomozygous652096607
4149422253149422254AT22GENIChomozygous652096608
4149422497149422498AG15GENIChomozygous652096609
4149422647149422648A-7GENICheterozygous758299105
4149425096149425097TG12GENIChomozygous652096610
4149425174149425175A-11GENIChomozygous758299106
4149425945149425946GA17GENIChomozygous652096611
4149426129149426134TTTTG-----16GENIChomozygous758299107
4149426288149426289AG21GENIChomozygous652096612
4149427447149427448CA30GENIChomozygous652096613