chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91022251410222515CT20GENIChomozygous938681181
91022284210222843CT18GENIChomozygous938681182
91022439010224391CA15GENIChomozygous938681183
91022637410226375AC18GENIChomozygous938681184
91022755610227557TC28GENIChomozygous938681185
91023050210230503AG23GENIChomozygous938681186
91023361210233613TG28GENIChomozygous938681187
91023446010234461AC28GENIChomozygous938681188
91023561510235616GC21GENIChomozygous938681189
91023912110239122AG26GENIChomozygous938681190
91023982010239821TC26GENIChomozygous938681191
91023983310239834GC26GENIChomozygous938681192
91023983510239836GC26GENIChomozygous938681193
91023984210239843AC25GENIChomozygous938681194
91023984510239846AC25GENIChomozygous938681195
91024309810243099TC20GENIChomozygous938681196
91024486110244862AG26GENIChomozygous938681197
91024592410245925TC23GENIChomozygous938681198
91024610910246110GT20GENIChomozygous938681199
91024859510248596CT15GENIChomozygous938681200
91024872610248727CT20GENIChomozygous938681201
91024957910249580AG21GENIChomozygous938681202
91024964710249648TC17GENIChomozygous938681203
91024999610249997CT21GENIChomozygous938681204
91025113810251139CT23GENIChomozygous938681205
91025374710253748AG16GENIChomozygous938681206
91025415110254152CG16GENIChomozygous938681207
91025571910255720CT25GENIChomozygous938681208
91025859510258596GT29GENIChomozygous938681209
91026048710260488CT21GENIChomozygous938681210
91026162810261629GC25GENIChomozygous938681211
91026706410267065AG12GENIChomozygous938681212
91026819110268192GA23GENIChomozygous938681213
91026852410268525AG10GENIChomozygous938681214
91027007010270071GA21GENIChomozygous938681215
91027011610270117TC13GENIChomozygous938681216
91027011810270119GA12GENIChomozygous938681217
91027020510270206TC4GENIChomozygous938681218
91027091810270919CT17GENIChomozygous938681219
91027117910271180TC15GENIChomozygous938681220
91027947210279473TC13GENIChomozygous938681221