| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27251783-27251936 | Common:2; Rare:51 | ||||
| chr13:27270602-27270654 | Rare:13 | ||||
| chr13:27270675-27270878 | Common:1; Rare:76 | ||||
| chr13:27271101-27271182 | Common:1; Rare:26 | ||||
| chr13:27424454-27424753 | Common:5; Rare:104 | ||||
| chr13:27424791-27424804 | Rare:3 | ||||
| chr13:27424821-27425008 | Common:1; Rare:60 | ||||
| chr13:27449914-27450339 | Common:3; Rare:130 | ||||
| chr13:27450343-27450781 | Common:4; Rare:150 | ||||
| chr13:27450981-27451071 | Rare:22 | ||||
| chr13:27620009-27620063 | Common:1; Rare:15 | ||||
| chr13:27620149-27620209 | Common:3; Rare:9 | ||||
| chr13:27620423-27621242 | Common:7; Rare:271 | ||||
| chr13:27621287-27621512 | Common:2; Rare:55 | ||||
| chr13:27621542-27621955 | Common:7; Rare:165; Clinvar:5; Clinvar (benign):5 |