chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177603210177603211GA7GENICheterozygous60969170
1177603640177603641GA3GENICheterozygous60969172
1177604146177604147TC20GENICpossibly homozygous60969174
1177606006177606007CT7GENICpossibly homozygous60969176
1177606686177606687CA6GENICheterozygous60969178
1177607561177607562AT17GENIChomozygous60969180
1177612088177612089AG23GENICpossibly homozygous60969184
1177612817177612818CT18GENICpossibly homozygous60969188
1177613540177613541CT15GENICpossibly homozygous60969190
1177614914177614915CT18GENICheterozygous60969192
1177614961177614962TC8GENIChomozygous60969194
1177615613177615614TTGG3GENIChomozygous60969196
1177615797177615798TC19GENICpossibly homozygous60969198
1177616646177616647AG18GENIChomozygous60969200
1177616722177616723CA19GENIChomozygous60969202
1177616913177616914CT29GENIChomozygous60969204
1177617680177617681CT3GENICheterozygous60969206
1177619932177619933AG10GENICpossibly homozygous60969208
1177621036177621037C-8GENIChomozygous60969210
1177621195177621196G-14GENIChomozygous60969212
1177621691177621692CT18GENICpossibly homozygous60969214
1177622060177622061CT15GENIChomozygous60969216
1177622212177622213CT12GENICpossibly homozygous60969218
1177624883177624884CT22GENICpossibly homozygous60969220
1177625104177625105CT23GENIChomozygous60969222
1177626672177626673TG15GENICpossibly homozygous60969224
1177627461177627462GA17GENIChomozygous60969225
1177628609177628610TC8GENICpossibly homozygous60969229
1177628848177628849AAAC6GENIChomozygous60969231
1177628953177628954G-2GENICheterozygous61561620
1177631429177631430CT15GENIChomozygous60969233
1177632309177632310GA13GENICpossibly homozygous60969235
1177634420177634421GA18GENICpossibly homozygous60969239