| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:24512399-24512907 | Common:4; Rare:130 | ||||
| chr13:24922482-24922609 | Rare:32 | ||||
| chr13:24922691-24923187 | Common:3; Rare:152; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:25287179-25287615 | Common:2; Rare:139 | ||||
| chr13:25301439-25301751 | Common:2; Rare:110 | ||||
| chr13:26221689-26222072 | Common:2; Rare:112 | ||||
| chr13:26222135-26222613 | Common:8; Rare:123 | ||||
| chr13:26254042-26254203 | Rare:40 | ||||
| chr13:27171004-27171301 | Common:3; Rare:74 | ||||
| chr13:27171685-27172176 | Common:1; Rare:174 | ||||
| chr13:27172317-27172391 | Rare:19 | ||||
| chr13:27251163-27251653 | Common:8; Rare:159 | ||||
| chr13:27270656-27270860 | Common:1; Rare:73 | ||||
| chr13:27424432-27424773 | Common:5; Rare:117 | ||||
| chr13:27449958-27450797 | Common:7; Rare:276 |