chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1217217891721789CA16GENIChomozygous144912116
1217218191721819CG11GENIChomozygous144912117
1217221081722109TC20GENIChomozygous139061482
1217226351722636AG17GENIChomozygous139061483
1217226871722688GC20GENIChomozygous139061484
1217227691722770AG17GENIChomozygous144915428
1217229121722913CT18GENIChomozygous139061486
1217232541723254TT22GENIChomozygous144912118
1217232731723274CT21GENIChomozygous139061487
1217234101723411TA4GENIChomozygous139061488
1217236031723604TG20GENICpossibly homozygous139061489
1217237741723775GA23GENIChomozygous144915429
1217233371723338AC10GENIChomozygous154753818
1217239551723956GA15GENIChomozygous144915430
1217253031725304TC16GENIChomozygous139061491
1217258671725868CT14GENIChomozygous139061492