chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171185660411856605TA25GENIChomozygous110958292
171185725311857254TC37GENIChomozygous110958294
171185748211857483AG14GENIChomozygous111168928
171185848011858481GA33GENIChomozygous110958296
171186004011860041AG36GENIChomozygous110958298
171186226211862263TG58GENIChomozygous110958300
171186301711863018CA50GENIChomozygous110958302
171186397211863973GA36GENIChomozygous110958304
171186486111864862AG34GENIChomozygous110958306
171186611011866111CT46GENIChomozygous110958308
171186725111867252TC64GENIChomozygous110958310
171187037711870378TG36GENIChomozygous111168930
171187173911871740CA46GENIChomozygous110958312
171187745011877451CT54GENIChomozygous110958314
171187995211879953GA58GENIChomozygous110958316
171187995811879959CT57GENIChomozygous110958318
171188111611881117GA27GENIChomozygous110958320
171188195011881951AG38GENIChomozygous110958322
171188260211882603CT31GENIChomozygous110958325
171188261011882611GA32GENIChomozygous110958327
171188337011883371GA29GENICpossibly homozygous111295153
171188418411884185GA35GENIChomozygous110958329
171188441411884415CT49GENIChomozygous110958331
171188524511885246GT52GENIChomozygous110958333
171188589111885892TC26GENIChomozygous110958335
171188680411886805GA43GENIChomozygous110958337
171188805611888057CT57GENIChomozygous110958339
171188978011889781GA45GENIChomozygous110958341
171189087311890874CT46GENIChomozygous110958343
171189108811891089GA58GENICpossibly homozygous111231292
171189275711892758AG47GENICpossibly homozygous110958345
171189329911893300TC59GENIChomozygous110958347
171189356711893568TC56GENIChomozygous110958348
171189104011891041GA56GENICheterozygous119264813