| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27450137-27450210 | Common:2; Rare:20 | ||||
| chr13:27450529-27450685 | Common:2; Rare:58 | ||||
| chr13:27620416-27620810 | Common:3; Rare:136 | ||||
| chr13:28137928-28138224 | Common:4; Rare:72 | ||||
| chr13:28659071-28659187 | Rare:49; Clinvar (pathogenic):1 | ||||
| chr13:29850121-29850225 | Rare:30 | ||||
| chr13:30306836-30307227 | Common:6; Rare:111 | ||||
| chr13:30307383-30307546 | Common:2; Rare:58 | ||||
| chr13:30617567-30618039 | Common:1; Rare:146 | ||||
| chr13:30735377-30735608 | Common:2; Rare:47 | ||||
| chr13:31162204-31162473 | Common:1; Rare:84 | ||||
| chr13:32586236-32586582 | Common:2; Rare:103 | ||||
| chr13:33285687-33285938 | Common:1; Rare:55 | ||||
| chr13:33818011-33818171 | Common:1; Rare:65 | ||||
| chr13:36346238-36346469 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 |