| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:24272633-24272711 | Common:3; Rare:8 | ||||
| chr13:24273162-24273279 | Common:1; Rare:23 | ||||
| chr13:24512385-24512609 | Common:3; Rare:61 | ||||
| chr13:24512646-24512905 | Common:3; Rare:67 | ||||
| chr13:24922708-24923157 | Common:2; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:25171717-25171825 | Common:1; Rare:27 | ||||
| chr13:25172134-25172238 | Rare:15 | ||||
| chr13:25172241-25172335 | Rare:7 | ||||
| chr13:25287165-25287697 | Common:4; Rare:160 | ||||
| chr13:25301044-25301091 | Rare:15 | ||||
| chr13:25301442-25301727 | Common:1; Rare:103 | ||||
| chr13:25301829-25301929 | Common:4; Rare:53 | ||||
| chr13:26221667-26222047 | Common:1; Rare:110 | ||||
| chr13:26222135-26222605 | Common:7; Rare:122 | ||||
| chr13:26253793-26253987 | Rare:52 |