| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110567260-110567830 | Common:4; Rare:192; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110567895-110567993 | Common:2; Rare:21 | ||||
| chr10:110568191-110568327 | Common:3; Rare:34 | ||||
| chr10:110871728-110871985 | Rare:83 | ||||
| chr10:110872214-110872320 | Rare:25 | ||||
| chr10:110918503-110918812 | Common:3; Rare:89 | ||||
| chr10:110918862-110918970 | Common:1; Rare:32 | ||||
| chr10:110919081-110919730 | Common:8; Rare:180; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:110919736-110919814 | Rare:25 | ||||
| chr10:112183657-112183951 | Common:3; Rare:99 | ||||
| chr10:112375131-112375385 | Common:2; Rare:45 | ||||
| chr10:112375955-112376309 | Rare:61 | ||||
| chr10:112376577-112376669 | Common:2; Rare:19 | ||||
| chr10:112446839-112447353 | Common:3; Rare:133 | ||||
| chr10:112447532-112447586 | Rare:10 |