| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:23889345-23889556 | Common:1; Rare:73 | ||||
| chr13:24512732-24512873 | Common:3; Rare:43 | ||||
| chr13:24922790-24923046 | Common:1; Rare:82; Clinvar:1 | ||||
| chr13:25287295-25287584 | Common:2; Rare:81 | ||||
| chr13:25301492-25301714 | Common:1; Rare:83 | ||||
| chr13:26221798-26221972 | Rare:51 | ||||
| chr13:26222258-26222377 | Common:2; Rare:34 | ||||
| chr13:27251225-27251617 | Common:8; Rare:122 | ||||
| chr13:27424499-27424711 | Common:4; Rare:70 | ||||
| chr13:27450113-27450222 | Common:3; Rare:34 | ||||
| chr13:27450392-27450657 | Common:4; Rare:105 | ||||
| chr13:28138117-28138200 | Rare:26 | ||||
| chr13:28659071-28659182 | Rare:48; Clinvar (pathogenic):1 | ||||
| chr13:28718951-28719123 | Common:1; Rare:37 | ||||
| chr13:30306828-30306967 | Common:1; Rare:44 |