chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142949682142949683CT58GENIChomozygous108264488
1142950005142950006GA43GENIChomozygous108264490
1142950864142950865CT44GENIChomozygous108264492
1142954896142954897AG33GENIChomozygous108264494
1142965918142965919GT39GENIChomozygous108264496
1142969312142969313CT35GENIChomozygous108264500
1142971003142971004GA44GENIChomozygous108264502
1142972882142972883AG54GENIChomozygous108264504
1142973858142973859TG54GENIChomozygous108264506
1142975275142975276AG30GENIChomozygous108264508
1142977323142977324TC35GENIChomozygous108264510
1142979281142979282AC57GENIChomozygous108264516
1142979291142979292GA62GENIChomozygous108264518
1142979480142979481GA43GENIChomozygous108264520
1142979489142979490TC39GENIChomozygous108264522
1142982285142982286AG49GENICpossibly homozygous108264525
1142984236142984237CA59GENIChomozygous108264527
1142987287142987288CT40GENIChomozygous108264529
1142990224142990225TC40GENIChomozygous108264531
1142990608142990609TC38GENIChomozygous108264533
1142991145142991146CT30GENIChomozygous108264535