chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15102493468102493469GT46GENIChomozygous112626305
15102493579102493580CT31GENIChomozygous112626307
15102493751102493752GT53GENIChomozygous112626309
15102494946102494947GA57GENIChomozygous112626311
15102495323102495324CA41GENIChomozygous112626313
15102495690102495691AT37GENIChomozygous112626315
15102496644102496645CT46GENIChomozygous112626317
15102496706102496707CT31GENIChomozygous112626319
15102496983102496984AG47GENICpossibly homozygous112626321