chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141627023816270239AAT24GENICheterozygous48953665
141627155916271560AG19GENIChomozygous48544550
141627159316271594GA18GENICheterozygous48544551
141627238416272385T-14GENIChomozygous48544552
141627263516272636AG15GENIChomozygous48544553
141627322416273225TC29GENIChomozygous48544554
141627327916273280CG31GENICpossibly homozygous48544555
141627435216274353AC21GENICheterozygous48544556
141627508716275088GA16GENICheterozygous48544557
141627810416278105TC14GENIChomozygous48544560
141628024016280241CG17GENICheterozygous49231085
141628074216280743AG8GENIChomozygous48544563
141628143716281438GA16GENICheterozygous48953669
141628144016281441CT18GENICheterozygous48953671
141628212116282122TC27GENICheterozygous48544564
141628221016282211TTAA18GENIChomozygous48544565
141628228216282283TTGGA11GENIChomozygous48544566
141628272916282730AC23GENICheterozygous48544567
141628371116283712AC21GENICheterozygous48544569
141628564916285650GA16GENICheterozygous48544570
141628638516286386TC11GENIChomozygous48544571
141628708416287085TC12GENIChomozygous48544576
141628763316287634GGCTGTCAGAAT10GENIChomozygous48544577
141628763516287636GGGA10GENIChomozygous48544578
141628855916288560CT13GENICheterozygous48953681