| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197736784-197737211 | Common:3; Rare:137 | ||||
| chr3:197749821-197749979 | Rare:67 | ||||
| chr3:197949894-197950247 | Common:4; Rare:108; Clinvar (benign):2 | ||||
| chr3:197959960-197960259 | Common:1; Rare:104 | ||||
| chr4:499141-499350 | Common:2; Rare:84 | ||||
| chr4:663604-663714 | Rare:33 | ||||
| chr4:673362-673625 | Common:1; Rare:95 | ||||
| chr4:673842-673948 | Rare:45 | ||||
| chr4:674212-674560 | Common:2; Rare:161 | ||||
| chr4:680416-680529 | Common:2; Rare:44 | ||||
| chr4:680829-681107 | Rare:85 | ||||
| chr4:705589-705851 | Rare:86 | ||||
| chr4:932064-932492 | Common:2; Rare:155 | ||||
| chr4:986930-987197 | Common:3; Rare:88; Clinvar:3; Clinvar (benign):3 | ||||
| chr4:1113524-1113630 | Common:2; Rare:38 |