Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52698070-52698239 | Common:1; Rare:51 | ||||
chr1:52698274-52698484 | Common:3; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:52927107-52927318 | Common:3; Rare:46 | ||||
chr1:53220515-53220691 | Common:2; Rare:87 | ||||
chr1:53238236-53238602 | Common:3; Rare:114 | ||||
chr1:53327902-53328259 | Common:2; Rare:95 | ||||
chr1:53838465-53838735 | Rare:63 | ||||
chr1:53889749-53889960 | Common:1; Rare:67 | ||||
chr1:53946253-53946491 | Rare:85 | ||||
chr1:54053172-54053687 | Common:6; Rare:170 | ||||
chr1:54199993-54200261 | Rare:80 | ||||
chr1:54715728-54715894 | Common:3; Rare:50 | ||||
chr1:54764481-54764820 | Common:7; Rare:95 | ||||
chr1:54887158-54887405 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
chr1:56579040-56579285 | Common:2; Rare:52 |