chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71244107012441071TC16GENIChomozygous53790948
71244178712441788G-12GENIChomozygous53790949
71244240812442409T-7GENIChomozygous53790951
71244280812442809AAC11GENICheterozygous53790952
71244302412443025TC17GENICpossibly homozygous53790954
71244315612443159TTT---7GENIChomozygous53790955
71244316012443161TG9GENICpossibly homozygous54884988
71244334412443345T-10GENIChomozygous53790956
71244360512443606CG12GENICheterozygous53790958
71244384112443842AAGGTG5GENIChomozygous53790959
71244434612444347TG14GENICheterozygous53790960
71244466712444668AG13GENIChomozygous53790961
71244514512445146CT11GENICpossibly homozygous53790962
71244522712445228TC21GENICpossibly homozygous53790963
71244540612445407TC10GENICpossibly homozygous53790964
71244549212445493TC8GENIChomozygous53790965
71244549512445496TG7GENIChomozygous53790966
71244550512445506CG9GENICheterozygous53790967
71244564412445645T-7GENIChomozygous53790968
71244612912446130TC19GENIChomozygous53790969
71244754012447541GT14GENICheterozygous53790973
71244840012448401CT19GENIChomozygous53790978
71244857512448576TC17GENIChomozygous53790979
71244872012448721GA23GENICpossibly homozygous53790980
71244904712449048AG27GENICpossibly homozygous53790981
71244994312449944CA16GENICpossibly homozygous53790982
71245007112450072CT6GENIChomozygous53790983
71245049912450500AG17INTERGENIChomozygous53790984
71245064312450644AAATAC6INTERGENIChomozygous53790985
71245080512450806CT29INTERGENICpossibly homozygous53790986
71245139512451396A-14INTERGENIChomozygous53790987
71245312212453123CT1GENIChomozygous53790988
71245332012453321GA10GENIChomozygous53790990
71245443612454437CCG1INTERGENIChomozygous53790991
71245507712455078TA21INTERGENICpossibly homozygous53790992
71245700212457003GA8INTERGENIChomozygous53790997