chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177604701177604702CT35GENIChomozygous532245195
1177607277177607278AG20GENIChomozygous532245196
1177607381177607393ATCATATATATA------------16GENIChomozygous693475899
1177607392177607393A-17GENIChomozygous693475900
1177607561177607562AT20GENIChomozygous529358527
1177612088177612089AG31GENIChomozygous529358528
1177612271177612272GA33GENIChomozygous532245197
1177615613177615614TTG19GENIChomozygous693475901
1177615797177615798TC22GENIChomozygous529358529
1177616646177616647AG19GENIChomozygous529358530
1177616722177616723CA17GENIChomozygous529358531
1177617481177617482CT37GENIChomozygous532245198
1177621036177621037C-23GENIChomozygous693475904
1177621195177621196G-19GENIChomozygous693475905
1177621691177621692CT17GENIChomozygous529358532
1177623302177623303AG44GENICheterozygous532245199
1177623313177623314TTAC38GENICheterozygous693475906
1177624883177624884CT13GENICpossibly homozygous529358533
1177626672177626673TG21GENIChomozygous529358534
1177627588177627589CCTT15GENIChomozygous693475908
1177627870177627871GA20GENIChomozygous532245200
1177628609177628610TC13GENIChomozygous529358535
1177628848177628849AAAC13GENIChomozygous693475909
1177628953177628954G-13GENIChomozygous693475912
1177632546177632558ACACACACACAT------------11GENICheterozygous693475913
1177634886177634887CT8GENIChomozygous532245201