Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:143513406-143514062 | Common:3; Rare:239 | ||||
chr4:145098107-145098348 | Rare:78 | ||||
chr4:145619327-145619402 | Rare:27 | ||||
chr4:147684088-147684235 | Common:1; Rare:54 | ||||
chr4:148442319-148442712 | Rare:111; Clinvar:4; Clinvar (benign):3 | ||||
chr4:150078722-150078836 | Common:1; Rare:31 | ||||
chr4:151015220-151015379 | Rare:45 | ||||
chr4:151099493-151099713 | Common:3; Rare:89 | ||||
chr4:151100292-151100584 | Common:1; Rare:58 | ||||
chr4:151408909-151409209 | Common:4; Rare:100 | ||||
chr4:152352694-152352854 | Rare:49 | ||||
chr4:152536054-152536407 | Common:2; Rare:135 | ||||
chr4:152779715-152779864 | Rare:43 | ||||
chr4:152779920-152780158 | Common:2; Rare:62 | ||||
chr4:153789081-153789178 | Rare:18 |