| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:24922790-24923024 | Common:1; Rare:72; Clinvar:1 | ||||
| chr13:26221791-26221990 | Rare:60 | ||||
| chr13:27251235-27251612 | Common:7; Rare:116 | ||||
| chr13:27424532-27424746 | Common:2; Rare:68 | ||||
| chr13:27450136-27450216 | Common:3; Rare:23 | ||||
| chr13:27450377-27450685 | Common:4; Rare:115 | ||||
| chr13:27620493-27620829 | Common:2; Rare:108 | ||||
| chr13:27621090-27621453 | Common:4; Rare:100 | ||||
| chr13:27967345-27967408 | Rare:11 | ||||
| chr13:28138139-28138234 | Common:1; Rare:28 | ||||
| chr13:28138661-28138910 | Common:1; Rare:62 | ||||
| chr13:28659073-28659194 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr13:28718521-28719123 | Common:4; Rare:141 | ||||
| chr13:29850290-29850419 | Common:2; Rare:42 | ||||
| chr13:29850436-29850478 | Common:1; Rare:8 |