chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177601966177601967CT19GENIChomozygous615885495
1177603210177603211GA18GENIChomozygous613616519
1177603640177603641GA35GENIChomozygous613616520
1177604146177604147TC29GENIChomozygous613616521
1177606006177606007CT20GENIChomozygous613616522
1177606686177606687CA25GENIChomozygous613616523
1177607561177607562AT32GENIChomozygous613616524
1177608614177608615CA26GENIChomozygous615885496
1177612088177612089AG26GENIChomozygous613616525
1177612162177612163CA21GENIChomozygous615885497
1177612817177612818CT34GENIChomozygous613616526
1177613540177613541CT30GENIChomozygous613616527
1177614914177614915CT37GENIChomozygous613616528
1177614961177614962TC24GENIChomozygous613616529
1177615613177615614TTGG14GENIChomozygous736025628
1177615797177615798TC18GENIChomozygous613616530
1177616646177616647AG33GENIChomozygous613616531
1177616722177616723CA30GENIChomozygous613616532
1177616913177616914CT34GENIChomozygous613616533
1177617680177617681CT37GENIChomozygous613616534
1177619932177619933AG30GENIChomozygous613616535
1177621036177621037C-24GENIChomozygous736025630
1177621195177621196G-32GENIChomozygous736025631
1177621691177621692CT43GENIChomozygous613616536
1177622060177622061CT23GENIChomozygous613616537
1177622212177622213CT42GENIChomozygous613616538
1177624883177624884CT44GENIChomozygous613616539
1177625104177625105CT27GENIChomozygous613616540
1177626672177626673TG23GENIChomozygous613616541
1177627461177627462GA34GENIChomozygous613616542
1177627588177627589CCT19GENICpossibly homozygous736025632
1177628609177628610TC43GENIChomozygous613616543
1177628848177628849AAAC16GENIChomozygous736025635
1177631429177631430CT24GENIChomozygous613616544
1177632309177632310GA33GENIChomozygous613616545
1177632548177632558ACACACACAT----------9GENIChomozygous736025636
1177634420177634421GA24GENIChomozygous613616546
1177634489177634491CC--6GENIChomozygous736025637