chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116732257116732258AG13GENIChomozygous116669999
8116734212116734213AG24GENIChomozygous116670003
8116735729116735730AG6GENIChomozygous116670007
8116736861116736862AG17GENIChomozygous116670013
8116738375116738375G13GENIChomozygous128635208
8116740312116740313AG20GENIChomozygous116670025
8116737839116737840CT14GENIChomozygous117149209
8116746767116746768CT20GENIChomozygous116670059
8116747054116747055CT12GENIChomozygous117149211
8116747711116747712CG14GENIChomozygous117149212
8116747885116747886GA21GENIChomozygous116670063
8116748143116748144CG13GENIChomozygous117149213
8116748664116748665GC15GENIChomozygous117149214
8116749214116749215AG14GENIChomozygous117149215
8116749399116749400AG19GENIChomozygous117149216
8116749414116749415CT14GENIChomozygous117149217
8116749994116749995AG14GENIChomozygous116670071
8116750338116750339AT20GENIChomozygous116670073
8116747442116747443TG4GENICheterozygous131061469
8116747437116747438AT4GENIChomozygous118150733
8116747439116747441AC4GENICheterozygous131054201
8116747444116747446AG4GENICheterozygous131054202
8116747449116747451CA4GENICheterozygous131054203
8116749962116749962TCCCCTC12GENIChomozygous131054204