| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:20566811-20567197 | Common:1; Rare:109 | ||||
| chr13:21176545-21176708 | Common:1; Rare:80 | ||||
| chr13:21670915-21671162 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:23579238-23579411 | Common:3; Rare:55 | ||||
| chr13:23889298-23889591 | Common:1; Rare:103 | ||||
| chr13:24512732-24512843 | Common:3; Rare:34 | ||||
| chr13:24922830-24923039 | Common:1; Rare:66; Clinvar:1 | ||||
| chr13:25301467-25301688 | Common:1; Rare:88 | ||||
| chr13:26221791-26221995 | Rare:60 | ||||
| chr13:27251243-27251623 | Common:6; Rare:115 | ||||
| chr13:27424516-27424830 | Common:2; Rare:104 | ||||
| chr13:27449968-27450220 | Common:3; Rare:75 | ||||
| chr13:27450336-27450621 | Common:4; Rare:107 | ||||
| chr13:27620443-27620805 | Common:2; Rare:121 | ||||
| chr13:28658948-28659184 | Rare:103; Clinvar (pathogenic):1 |