chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181870484181870485GA39GENIChomozygous506616447
4181871086181871087TC47GENICpossibly homozygous506616448
4181871589181871590AG42GENIChomozygous506616449
4181871907181871908CT51GENICpossibly homozygous510239360
4181872014181872015CT50GENIChomozygous510239361
4181872168181872169GT37GENIChomozygous510239362
4181872359181872360TC21GENIChomozygous510239363
4181872420181872421A-14GENIChomozygous685566291
4181872427181872428A-16GENIChomozygous685566292
4181872443181872444A-19GENIChomozygous685566293