chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1217217891721789CA18GENIChomozygous144912116
1217218191721819CG16GENIChomozygous144912117
1217221081722109TC14GENIChomozygous139061482
1217226351722636AG13GENIChomozygous139061483
1217226871722688GC15GENIChomozygous139061484
1217227691722770AG13GENIChomozygous144915428
1217229121722913CT20GENIChomozygous139061486
1217232541723254TT12GENIChomozygous144912118
1217232731723274CT11GENIChomozygous139061487
1217234101723411TA8GENIChomozygous139061488
1217236031723604TG7GENICpossibly homozygous139061489
1217237741723775GA14GENIChomozygous144915429
1217239551723956GA18GENIChomozygous144915430
1217233371723338AC7GENIChomozygous154753818
1217253031725304TC12GENIChomozygous139061491
1217258671725868CT11GENIChomozygous139061492