| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:112967802-112968479 | Common:11; Rare:191 | ||||
| chr13:112969083-112969394 | Common:6; Rare:209 | ||||
| chr13:112985500-112985990 | Common:10; Rare:161 | ||||
| chr13:113001120-113001410 | Common:2; Rare:69 | ||||
| chr13:113001421-113001829 | Common:3; Rare:242 | ||||
| chr13:113002243-113002471 | Common:4; Rare:65 | ||||
| chr13:113105370-113106003 | Common:13; Rare:301; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):4 | ||||
| chr13:113207723-113208441 | Common:9; Rare:342 | ||||
| chr13:113208577-113208827 | Rare:341 | ||||
| chr13:113208890-113209210 | Common:10; Rare:229 | ||||
| chr13:113209430-113209763 | Common:9; Rare:217 | ||||
| chr13:113209958-113210281 | Common:1; Rare:130 | ||||
| chr13:113243800-113244310 | Common:4; Rare:74 | ||||
| chr13:113296896-113297458 | Common:10; Rare:459 | ||||
| chr13:113364005-113364507 | Common:5; Rare:129 |