| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127081948-127082261 | Common:5; Rare:61 | ||||
| chr2:127084191-127084450 | Common:3; Rare:65 | ||||
| chr2:151492078-151492495 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:151493924-151494261 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:151496257-151496422 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr2:151496813-151497042 | Common:1; Rare:61; Clinvar:5; Clinvar (pathogenic):6 | ||||
| chr2:151498217-151498378 | Rare:39; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:151530992-151531380 | Common:6; Rare:68; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:151537872-151538060 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:151561002-151561315 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:151568069-151568417 | Rare:85; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:151610486-151610868 | Rare:106; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:151642572-151642899 | Common:3; Rare:86; Clinvar:4; Clinvar (benign):6 | ||||
| chr2:151679716-151680024 | Common:3; Rare:94; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:151680728-151680897 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):2 |