chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14108396672108396673CT29GENIChomozygous113541154
14108397829108397830GA38GENIChomozygous113541156
14108397982108397983AG40GENIChomozygous113541158
14108398890108398891GC29GENIChomozygous113541160
14108399314108399315GC23GENICpossibly homozygous113541162
14108399743108399744TA30GENIChomozygous113541164
14108400238108400239GC30GENIChomozygous113541166
14108400566108400567TA25GENIChomozygous113541168
14108400570108400571TA25GENIChomozygous113541170
14108400746108400747GA31GENIChomozygous113541172
14108400990108400991AG38GENIChomozygous113541174
14108401086108401087TG37GENIChomozygous113541176
14108401388108401389GA42GENIChomozygous113541178
14108402419108402420GA47GENIChomozygous113541180
14108403132108403133AG27GENIChomozygous113541184
14108403799108403800AG34GENIChomozygous113541186
14108404078108404079TG40GENIChomozygous113541188
14108404161108404162CT49GENIChomozygous113541190
14108404200108404201CG44GENIChomozygous113541194
14108404485108404486AC45GENIChomozygous113541196
14108405060108405061TC24GENIChomozygous113541198
14108405081108405082TC22GENIChomozygous113541200
14108405597108405598CT20GENIChomozygous113541202
14108406349108406350GT34GENIChomozygous113541204
14108406408108406409GC37GENIChomozygous113541206
14108406488108406489CT47GENIChomozygous113541208
14108406848108406849CT30GENIChomozygous113541212
14108407723108407724CG24GENIChomozygous113541216
14108408381108408382AG19GENIChomozygous113618353
14108408627108408628CT17GENIChomozygous113541219
14108409859108409860TC25GENIChomozygous113541221
14108410733108410734GA21GENIChomozygous113541223