chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166542176166542177CT10GENICpossibly homozygous780373687
5166548732166548733GA14GENIChomozygous780373688
5166549103166549104CT58GENIChomozygous780373689
5166559292166559293CT47GENICheterozygous780373690
5166559377166559378CG84GENICheterozygous780373691
5166559379166559380GT85GENICheterozygous780373692
5166559396166559397TG87GENICheterozygous780373693
5166576109166576110CT58GENICheterozygous780373694
5166586020166586021GA15GENICpossibly homozygous780373695
5166591468166591469GT32GENICpossibly homozygous780373696