chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151375746151375747GA21GENIChomozygous113244156
4151376138151376139TC9GENIChomozygous113244157
4151377755151377756CT12GENIChomozygous113244159
4151378277151378278AG25GENIChomozygous113244160
4151379337151379338CT15GENIChomozygous113244161
4151379950151379951AG10GENIChomozygous113244163
4151381912151381912T28GENIChomozygous132968197
4151381914151381914CTGCT27GENIChomozygous132968198
4151382149151382150CT12GENIChomozygous113244164
4151382945151382947TC3GENIChomozygous132968199
4151384010151384011CG16GENIChomozygous113244165
4151384684151384684C12GENIChomozygous132968200
4151386009151386010G13GENIChomozygous128091546
4151386519151386520AG12GENIChomozygous113244166
4151386772151386773AG23GENIChomozygous113244167
4151386959151386960GT15GENIChomozygous113244168
4151388443151388444AC24GENIChomozygous113244169
4151388782151388782C14GENIChomozygous132968201
4151390458151390459TG22GENIChomozygous113244170
4151390773151390774GA10GENIChomozygous113244171
4151391443151391447ACAC16GENIChomozygous128091547
4151393212151393213GA18GENIChomozygous113244173
4151395584151395592AACAGGGA17GENIChomozygous128091550
4151395655151395656GA21GENIChomozygous113244174
4151395714151395715CT22GENIChomozygous113244175
4151396212151396213G12GENIChomozygous132968202
4151396632151396633CT16GENIChomozygous113244176
4151396949151396950CT17GENIChomozygous113244177
4151397133151397134AC15GENIChomozygous113244178
4151397186151397186CACATGTATACCTGCACACAGAACATACATAC16GENIChomozygous133819543