chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14108396672108396673CT17GENIChomozygous113541154
14108397829108397830GA18GENIChomozygous113541156
14108397982108397983AG16GENIChomozygous113541158
14108398890108398891GC10GENIChomozygous113541160
14108399314108399315GC15GENIChomozygous113541162
14108399743108399744TA23GENIChomozygous113541164
14108400238108400239GC17GENIChomozygous113541166
14108400566108400567TA19GENIChomozygous113541168
14108400570108400571TA21GENIChomozygous113541170
14108400746108400747GA19GENIChomozygous113541172
14108400990108400991AG30GENIChomozygous113541174
14108401086108401087TG20GENIChomozygous113541176
14108401388108401389GA35GENIChomozygous113541178
14108401784108401785CT12GENICheterozygous114104040
14108402419108402420GA14GENIChomozygous113541180
14108402464108402465TC15GENIChomozygous113541182
14108403132108403133AG25GENIChomozygous113541184
14108403799108403800AG26GENIChomozygous113541186
14108404078108404079TG39GENIChomozygous113541188
14108404161108404162CT30GENIChomozygous113541190
14108404192108404193TA29GENIChomozygous113541192
14108404200108404201CG29GENIChomozygous113541194
14108404485108404486AC40GENIChomozygous113541196
14108405060108405061TC32GENIChomozygous113541198
14108405081108405082TC29GENIChomozygous113541200
14108405597108405598CT22GENIChomozygous113541202
14108406349108406350GT33GENIChomozygous113541204
14108406408108406409GC38GENIChomozygous113541206
14108406488108406489CT32GENIChomozygous113541208
14108406586108406587GA22GENIChomozygous113541210
14108406848108406849CT20GENIChomozygous113541212
14108407383108407384AG27GENIChomozygous113541214
14108407723108407724CG25GENIChomozygous113541216
14108408105108408106GA11GENIChomozygous113541217
14108408381108408382AG9GENIChomozygous113618353
14108408627108408628CT31GENIChomozygous113541219
14108409859108409860TC22GENIChomozygous113541221
14108410733108410734GA18GENIChomozygous113541223