chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1182417998182417999GC18GENICheterozygous153898815
1182417998182417999G18GENIChomozygous402974975
1182418000182418001GC18GENICheterozygous153898816
1182418000182418001G18GENIChomozygous402974976
1182420623182420624GT17GENIChomozygous143805179
1182424968182424969GA13GENIChomozygous143805180
1182425028182425029TC11GENIChomozygous143805181
1182425044182425045GA11GENIChomozygous143805182
1182427096182427097GT25GENIChomozygous143805183
1182427488182427489GT21GENIChomozygous143805184
1182429584182429585G10GENICheterozygous404335579
1182429584182429585GC10GENICheterozygous404335580
1182429586182429587G10GENICheterozygous404425664
1182429586182429587GC10GENICheterozygous404425665
1182429588182429589G10GENICheterozygous404425666
1182429588182429589GC10GENICheterozygous404425667
1182429590182429591G10GENICheterozygous404425668
1182429590182429591GC10GENICheterozygous404425669
1182433475182433476TA14GENICheterozygous153898822
1182433475182433476T14GENICheterozygous402974979
1182429592182429593GC9GENICheterozygous147448719
1182428406182428407C7GENIChomozygous135449327
1182431375182431377AC11GENIChomozygous143744650
1182433466182433476CACACACACT14GENICheterozygous147392319