| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:103396386-103396702 | Rare:116 | ||||
| chr10:103452246-103452453 | Rare:60 | ||||
| chr10:103918120-103918523 | Common:5; Rare:110 | ||||
| chr10:104268956-104269212 | Common:4; Rare:61 | ||||
| chr10:109923423-109923660 | Common:2; Rare:91 | ||||
| chr10:109996234-109996397 | Rare:25 | ||||
| chr10:110005899-110006106 | Common:4; Rare:59 | ||||
| chr10:110007668-110008280 | Common:2; Rare:201 | ||||
| chr10:110567922-110567980 | Rare:12 | ||||
| chr10:110871622-110871964 | Rare:111 | ||||
| chr10:110918937-110918958 | Rare:5 | ||||
| chr10:110919134-110919654 | Common:8; Rare:138; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:112183708-112183851 | Common:3; Rare:54 | ||||
| chr10:112446720-112447356 | Common:3; Rare:156 | ||||
| chr10:112950037-112950317 | Common:3; Rare:58 |