chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118526357118526358GC22GENIChomozygous947467248
8118527316118527317AC10GENIChomozygous947467249
8118527665118527666CT28GENIChomozygous947467250
8118527743118527744TC15GENIChomozygous947467251
8118528101118528102CG16GENIChomozygous947467252
8118528291118528292CT21GENIChomozygous947467253
8118528481118528482GA23GENIChomozygous947467254
8118528636118528637TC23GENIChomozygous947467255
8118529030118529031AG28GENIChomozygous947467256
8118529158118529159AG17GENIChomozygous947467257
8118529804118529805AG20GENIChomozygous947467258
8118530544118530545CT18GENIChomozygous947467259
8118533016118533017GA21GENIChomozygous947467260
8118533158118533159GA30GENIChomozygous947467261
8118533356118533357CT31GENIChomozygous947467262
8118533536118533537CT25GENICpossibly homozygous947467263
8118533605118533606GA28GENICpossibly homozygous947467264
8118534045118534046TC28GENIChomozygous947467265
8118534207118534208TC31GENIChomozygous947467266
8118534298118534299TC24GENIChomozygous947467267
8118535489118535490TC29GENIChomozygous947467268
8118536494118536495AC14GENIChomozygous947467269
8118536972118536973GA29GENIChomozygous947467270
8118539078118539079CT32GENIChomozygous947467271
8118539122118539123TC29GENIChomozygous947467272
8118539275118539276TC21GENIChomozygous947467273
8118539339118539340TC15GENIChomozygous947467274
8118539596118539597AT22GENIChomozygous947467275
8118539990118539991CT26GENICpossibly homozygous947467276
8118540242118540243GT23GENIChomozygous947467277
8118540755118540756TG17GENIChomozygous947467278