chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143649841143649842GA17GENIChomozygous555885111
5143650275143650276CT19GENIChomozygous555885112
5143650874143650875T-9GENIChomozygous705031889
5143652921143652922CCT14GENIChomozygous705031890
5143653053143653054TA12GENIChomozygous557934332
5143653704143653706TT--5GENICheterozygous705031891
5143653705143653706T-5GENICheterozygous705031892
5143653825143653828TTT---7GENIChomozygous705031893
5143653991143653992AG13GENIChomozygous557934333
5143654022143654023CT13GENIChomozygous555885113
5143654077143654078TA6GENIChomozygous557934334
5143654078143654079TA6GENIChomozygous557934335
5143654080143654081TA7GENIChomozygous557934336
5143654087143654088TTA6GENIChomozygous705031895
5143654168143654169AG17GENIChomozygous555885114
5143654180143654181CG19GENIChomozygous555885115
5143654658143654659AG12GENIChomozygous555885116
5143656319143656320TC33GENIChomozygous555885117
5143657627143657628AAC8GENIChomozygous705031896
5143657632143657634GC--7GENIChomozygous705031897
5143657643143657644TTC7GENIChomozygous705031898
5143657653143657654A-6GENIChomozygous705031899
5143657656143657658CT--5GENIChomozygous705031900
5143657836143657837G-10GENIChomozygous705031901
5143659534143659536TA--2GENIChomozygous705031902
5143659541143659551TTATTATTAT----------2GENIChomozygous705031903
5143663154143663155TTTGTG2GENIChomozygous705031907
5143663904143663905AG15GENIChomozygous555885118
5143664036143664037A-8GENIChomozygous705031910
5143664037143664038AT8GENIChomozygous557934337
5143664360143664364ATGT----10GENIChomozygous705031912
5143664536143664537AG18GENIChomozygous555885119