chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2067588776758878CT39INTERGENICheterozygous63694370
2067590206759021GA26INTERGENIChomozygous63644178
2067594516759452GT31INTERGENICpossibly homozygous63644179
2067595526759553CT33INTERGENIChomozygous63347436
2067604196760420CG28INTERGENICpossibly homozygous63644180
2067609316760932AG34INTERGENIChomozygous63347442
2067620526762053TC33INTERGENIChomozygous63347446
2067635656763566CA19INTERGENIChomozygous63644181
2067646276764628GA35INTERGENIChomozygous63347454
2067646896764690CA36INTERGENIChomozygous63644182
2067647176764718CG28INTERGENIChomozygous63347458
2067652316765232AG23INTERGENIChomozygous63644183
2067654936765494CT19INTERGENICheterozygous63644184
2067656516765652GA34INTERGENICheterozygous63644185
2067683836768384CA28INTERGENIChomozygous63347467
2067686726768673AG28INTERGENIChomozygous63347469
2067688186768819AC17INTERGENICheterozygous63347471
2067692226769223CT24INTERGENIChomozygous63644187
2067707546770755AG26GENIChomozygous63347475
2067715996771600GA32GENIChomozygous63644188
2067716116771612TC24GENIChomozygous63644189
2067716186771619GA20GENIChomozygous63644190
2067724006772401CG43GENIChomozygous63347479
2067733986773399TG28GENICpossibly homozygous63644197
2067718166771817CG13GENICpossibly homozygous63644191
2067723386772339TC41GENIChomozygous63644192
2067724376772438CA42GENIChomozygous63644193
2067724696772470AG28GENIChomozygous63644194
2067726556772656TG59GENIChomozygous63644195
2067732596773260AG43GENICheterozygous63644196
2067753156775316AG10GENICpossibly homozygous63644198
2067759976775998TC22GENIChomozygous63644199
2067764906776491CT39GENIChomozygous63644200
2067769436776944TA34GENIChomozygous63644201
2067775556777556CG27GENICheterozygous63694372
2067775946777595AT13GENIChomozygous63644202
2067780706778071GA24GENIChomozygous63347483
2067781386778139CT46GENIChomozygous63644203
2067786806778681CT44GENIChomozygous63644204