chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2203922503203922504AT52GENIChomozygous146682546
2203922837203922838GA57GENIChomozygous146682547
2203928013203928014CA64GENIChomozygous136446036
2203924795203924796CT50GENIChomozygous136446031
2203929216203929217CT54GENIChomozygous146682548
2203929800203929801GA51GENIChomozygous146682549
2203932269203932270TC56GENIChomozygous136446038
2203933649203933650CA54GENIChomozygous136446040
2203934050203934051AG41GENIChomozygous136446041
2203934870203934871CT44GENIChomozygous146682550
2203934985203934986CG49GENIChomozygous136446042
2203935801203935802GA31GENIChomozygous136446043
2203936767203936768AG32GENIChomozygous146682551
2203939530203939531AG37GENIChomozygous136446045
2203940030203940031GA36GENIChomozygous136446046
2203943820203943821TC45GENIChomozygous136446047
2203944048203944049TC42GENIChomozygous136446048
2203944407203944408TC48GENIChomozygous136446049
2203944876203944877GA56GENIChomozygous146682552
2203944991203944992GA45GENIChomozygous136446050
2203946632203946633TC54GENIChomozygous136446051
2203946773203946774GA66GENIChomozygous136446052
2203941105203941109TTTC9GENICheterozygous146642989
2203940811203940812A42GENIChomozygous146642988