chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3114721511114721512CA28GENICpossibly homozygous125833248
3114721712114721713GT10GENIChomozygous125833254
3114721796114721797CT14GENIChomozygous111680184
3114721832114721833CG11GENIChomozygous112140532
3114722255114722256CT5GENIChomozygous111680186
3114722517114722518TC25GENIChomozygous112140533
3114722584114722585CT20GENIChomozygous112140534
3114722627114722628CT15GENIChomozygous112140535
3114722944114722945AG9GENIChomozygous111680188
3114723642114723643TC6GENIChomozygous112140537
3114723649114723650TC5GENIChomozygous112140538
3114723814114723815CT4GENIChomozygous125894389
3114723857114723858AG11GENIChomozygous112140539
3114724148114724149TC15GENIChomozygous112140540
3114724249114724250AC13GENIChomozygous112140541
3114724379114724380CG25GENIChomozygous112140542
3114724710114724711CT24GENIChomozygous112140543
3114724794114724795TC29GENIChomozygous111680191
3114724874114724875CT20GENIChomozygous112140544
3114725243114725244CG19GENIChomozygous112140545
3114725495114725496CA17GENIChomozygous112140546
3114725588114725589GA21GENIChomozygous112140547
3114726577114726578GA10GENIChomozygous112140548