chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177603210177603211GA72GENIChomozygous60969170
1177603640177603641GA61GENIChomozygous60969172
1177604146177604147TC33GENIChomozygous60969174
1177606006177606007CT26GENIChomozygous60969176
1177606686177606687CA81GENIChomozygous60969178
1177607561177607562AT15GENIChomozygous60969180
1177612088177612089AG75GENIChomozygous60969184
1177612817177612818CT38GENIChomozygous60969188
1177613540177613541CT83GENIChomozygous60969190
1177614914177614915CT39GENIChomozygous60969192
1177614961177614962TC62GENIChomozygous60969194
1177615613177615614TTGGG16GENIChomozygous61561617
1177615797177615798TC27GENIChomozygous60969198
1177616646177616647AG14GENIChomozygous60969200
1177616722177616723CA16GENIChomozygous60969202
1177616913177616914CT35GENIChomozygous60969204
1177617680177617681CT44GENIChomozygous60969206
1177619932177619933AG74GENIChomozygous60969208
1177621036177621037C-30GENIChomozygous60969210
1177621195177621196G-32GENIChomozygous60969212
1177621691177621692CT39GENIChomozygous60969214
1177622060177622061CT42GENIChomozygous60969216
1177622212177622213CT30GENIChomozygous60969218
1177624883177624884CT28GENIChomozygous60969220
1177625104177625105CT13GENIChomozygous60969222
1177626672177626673TG32GENIChomozygous60969224
1177627461177627462GA44GENIChomozygous60969225
1177627588177627589CCTT3GENICheterozygous60969227
1177628609177628610TC18GENIChomozygous60969229
1177628849177628853ACAC----34GENIChomozygous61561618
1177628952177628953TTG7GENICpossibly homozygous61561619
1177631429177631430CT30GENIChomozygous60969233
1177632309177632310GA16GENIChomozygous60969235
1177632546177632558ACACACACACAT------------9GENICheterozygous60969237
1177634280177634281TA54GENIChomozygous61561621
1177634420177634421GA93GENIChomozygous60969239
1177634489177634491CC--37GENIChomozygous60969241
1177627588177627589CCT3GENICheterozygous62178628