chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177601966177601967CT18GENIChomozygous671852801
1177603210177603211GA21GENIChomozygous671852802
1177603640177603641GA26GENIChomozygous671852803
1177604146177604147TC30GENIChomozygous671852804
1177606006177606007CT21GENIChomozygous671852805
1177606686177606687CA17GENIChomozygous671852806
1177607561177607562AT16GENIChomozygous671852807
1177608614177608615CA26GENICpossibly homozygous671852808
1177612088177612089AG29GENIChomozygous671852809
1177612162177612163CA20GENIChomozygous671852810
1177612817177612818CT26GENIChomozygous671852811
1177613540177613541CT32GENIChomozygous671852812
1177614914177614915CT26GENIChomozygous671852813
1177614961177614962TC27GENIChomozygous671852814
1177615613177615614TTGG21GENIChomozygous769234856
1177615797177615798TC20GENIChomozygous671852815
1177616646177616647AG18GENIChomozygous671852816
1177616722177616723CA17GENIChomozygous671852817
1177616913177616914CT31GENIChomozygous671852818
1177617680177617681CT20GENIChomozygous671852819
1177619932177619933AG21GENIChomozygous671852820
1177621036177621037C-23GENIChomozygous769234858
1177621195177621196G-31GENIChomozygous769234859
1177621691177621692CT22GENIChomozygous671852821
1177622060177622061CT24GENIChomozygous671852822
1177622212177622213CT31GENIChomozygous671852823
1177624883177624884CT29GENIChomozygous671852824
1177625104177625105CT40GENIChomozygous671852825
1177626672177626673TG34GENIChomozygous671852826
1177627461177627462GA22GENIChomozygous671852827
1177627588177627589CCT12GENICheterozygous769234860
1177627588177627589CCTT12GENICheterozygous769234861
1177628609177628610TC32GENIChomozygous671852828
1177628848177628849AAAC25GENIChomozygous769234863
1177628953177628954G-5GENICheterozygous769234864
1177631429177631430CT23GENIChomozygous671852829
1177632309177632310GA26GENIChomozygous671852830
1177632548177632558ACACACACAT----------10GENICpossibly homozygous769234866
1177634420177634421GA18GENIChomozygous671852831
1177634489177634491CC--5GENIChomozygous769234867