chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264160581264160582CT61GENICpossibly homozygous108635352
1264160723264160724AG64GENIChomozygous108635354
1264162008264162009AG56GENIChomozygous108635356
1264163548264163549TC67GENIChomozygous120905127
1264165040264165041TC68GENIChomozygous108635365
1264166044264166045AG70GENICpossibly homozygous108635370
1264166583264166584GA64GENIChomozygous120905128
1264168064264168065CT53GENIChomozygous120905129
1264168272264168273TC70GENIChomozygous108635397
1264163798264163799GA69GENIChomozygous135147841
1264164198264164199G57GENIChomozygous127508530
1264169506264169507CT56GENICpossibly homozygous108635416
1264170041264170042GA76GENIChomozygous120905130
1264171365264171365A42GENICheterozygous132543190
1264171838264171839AG57GENIChomozygous108635437
1264172274264172275AG58GENIChomozygous108635439
1264172417264172418AC68GENICpossibly homozygous108635441
1264172950264172950AGGGAGGGAGGT27GENICpossibly homozygous127508535
1264172985264172986AG33GENIChomozygous108635447