chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31538474315384744TC16GENIChomozygous136643096
31538534815385349GA19GENIChomozygous136643097
31538537415385375TA18GENICpossibly homozygous136643098
31538611915386120AG16GENIChomozygous136643099
31538817715388178CT15GENIChomozygous136643100
31538818215388183AC15GENIChomozygous136643101
31538834515388346GA18GENIChomozygous136643102
31538900715389008AG14GENIChomozygous136643103
31538901015389011CA14GENIChomozygous136643104
31539101315391014T9GENIChomozygous403057681
31539101315391014TC9GENICheterozygous403057682
31539228715392288TC18GENIChomozygous136643105
31539339415393395TC13GENIChomozygous136643106
31539345915393460TC10GENIChomozygous136643107
31539358215393583CT18GENIChomozygous136643108
31539363615393637TC24GENIChomozygous136643109
31539469815394699GC22GENIChomozygous136643110
31539490815394908GAGTAT23GENIChomozygous136549554
31538903815389043GAAGA17GENIChomozygous136549551
31538980215389803A22GENIChomozygous136549552
31539100815391014TCCTCT9GENIChomozygous136549553
31539524215395243GC28GENIChomozygous136643114
31539507215395073GA17GENIChomozygous136643111
31539511115395112TG21GENIChomozygous136643112
31539511615395117CT21GENIChomozygous136643113
31539537615395377AG15GENIChomozygous136643115
31539701315397016AAG11GENIChomozygous141471481
31539701515397016G11GENIChomozygous403057684
31539701515397016GA11GENICheterozygous403057685
31539822215398223CA11GENIChomozygous136643119
31539571315395714AC25GENIChomozygous136643116
31539639115396392CT17GENIChomozygous136643117
31539820115398202TA14GENIChomozygous136643118
31539822315398224CT11GENIChomozygous136643120
31539839315398394CT20GENIChomozygous136643121