| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:43879630-43880150 | Common:41; Rare:217 | ||||
| chr13:44436823-44437010 | Common:4; Rare:118 | ||||
| chr13:44577255-44577398 | Common:1; Rare:47 | ||||
| chr13:44989414-44989607 | Rare:155 | ||||
| chr13:45120383-45120573 | Common:3; Rare:118 | ||||
| chr13:45341042-45341657 | Common:8; Rare:510 | ||||
| chr13:45418318-45418578 | Rare:148 | ||||
| chr13:45464641-45465133 | Common:2; Rare:226 | ||||
| chr13:45465210-45465570 | Common:2; Rare:157 | ||||
| chr13:46052714-46052842 | Common:3; Rare:56 | ||||
| chr13:46553026-46553400 | Common:6; Rare:175 | ||||
| chr13:46797099-46797263 | Common:4; Rare:110 | ||||
| chr13:46797620-46797970 | Common:1; Rare:112 | ||||
| chr13:48001228-48001473 | Common:4; Rare:175; Clinvar:6; Clinvar (benign):10 | ||||
| chr13:48037571-48037801 | Common:1; Rare:158; Clinvar:1 |