chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18617612286176123TC38GENICheterozygous153865703
18617612286176123T38GENICheterozygous402951756
18617612486176125TC38GENICheterozygous153865704
18617612486176125T38GENICheterozygous402951757
18617814786178148AG57GENIChomozygous142843194
18617905986179060TG50GENIChomozygous142843195
18618024086180241T25GENICpossibly homozygous402951762
18618024086180241TG25GENICheterozygous402951763
18618090686180907CG34GENIChomozygous142843196
18618246686182467TC62GENIChomozygous142843197
18618023386180238TTTGT19GENICheterozygous142790390