chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142949682142949683CT68GENIChomozygous108264488
1142950005142950006GA45GENIChomozygous108264490
1142950864142950865CT48GENIChomozygous108264492
1142954896142954897AG38GENIChomozygous108264494
1142965918142965919GT49GENIChomozygous108264496
1142967805142967806AG38GENICheterozygous108264498
1142969312142969313CT40GENIChomozygous108264500
1142971003142971004GA51GENIChomozygous108264502
1142972882142972883AG56GENIChomozygous108264504
1142973858142973859TG60GENIChomozygous108264506
1142975275142975276AG36GENICpossibly homozygous108264508
1142977323142977324TC42GENIChomozygous108264510
1142977498142977499GT21GENIChomozygous108264512
1142977521142977522CG18GENICheterozygous108264514
1142979281142979282AC64GENIChomozygous108264516
1142979291142979292GA68GENIChomozygous108264518
1142979480142979481GA48GENIChomozygous108264520
1142979489142979490TC46GENIChomozygous108264522
1142980278142980279TA36GENICpossibly homozygous108264523
1142982285142982286AG52GENICpossibly homozygous108264525
1142984236142984237CA74GENIChomozygous108264527
1142987287142987288CT43GENICpossibly homozygous108264529
1142990224142990225TC44GENIChomozygous108264531
1142990608142990609TC38GENIChomozygous108264533
1142991145142991146CT43GENICpossibly homozygous108264535