chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221910817221910818AC17GENIChomozygous108545523
1221910854221910855GT25GENIChomozygous108545525
1221912789221912790AG25GENIChomozygous108545527
1221912883221912884CT17GENICpossibly homozygous108545529
1221913397221913398AG14GENIChomozygous108545531
1221913485221913486CT19GENIChomozygous108545533
1221913876221913877GA17GENIChomozygous108545535
1221915026221915027AC23GENIChomozygous108545537
1221916552221916553TA6GENIChomozygous108545539
1221916680221916681AG4GENIChomozygous108545541
1221918902221918903AG16GENIChomozygous108545543