chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142950864142950865CT20GENIChomozygous108264492
1142952860142952861CT8GENIChomozygous109328192
1142952943142952944AG11GENIChomozygous109328194
1142954896142954897AG10GENICheterozygous108264494
1142958616142958617GT4GENICheterozygous120781365
1142960706142960707TC8GENIChomozygous109328198
1142963611142963612GA16GENIChomozygous109328199
1142964140142964141TC3GENICheterozygous125430241
1142965855142965856CT23GENIChomozygous109328201
1142965918142965919GT20GENIChomozygous108264496
1142969312142969313CT18GENICheterozygous108264500
1142972882142972883AG17GENIChomozygous108264504
1142973858142973859TG18GENIChomozygous108264506
1142975275142975276AG5GENIChomozygous108264508
1142977323142977324TC22GENIChomozygous108264510
1142979281142979282AC14GENIChomozygous108264516
1142979489142979490TC14GENIChomozygous108264522
1142981230142981231AC7GENIChomozygous109328202
1142981259142981260GC5GENICheterozygous109518055
1142981708142981709GT4GENIChomozygous109328208
1142982285142982286AG9GENIChomozygous108264525
1142984236142984237CA27GENIChomozygous108264527
1142987287142987288CT17GENIChomozygous108264529
1142988814142988815CT22GENIChomozygous109328210
1142990013142990014GA11GENIChomozygous109328211
1142990325142990326TC7GENIChomozygous109328213
1142990608142990609TC11GENIChomozygous108264533
1142991323142991324GA15GENIChomozygous109328219
1142991203142991204AG19GENIChomozygous109328217
1142991471142991472GA19GENIChomozygous109328220
1142992184142992185CG12GENIChomozygous108937989