| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:104254832-104254946 | Rare:34 | ||||
| chr10:104268745-104268847 | Common:1; Rare:20 | ||||
| chr10:104268850-104269223 | Common:6; Rare:89 | ||||
| chr10:104275119-104275190 | Rare:16 | ||||
| chr10:104338456-104338549 | Rare:21 | ||||
| chr10:104353592-104353834 | Common:2; Rare:65 | ||||
| chr10:109923420-109923672 | Common:2; Rare:98 | ||||
| chr10:109996161-109996428 | Rare:45 | ||||
| chr10:110005894-110006117 | Common:4; Rare:63 | ||||
| chr10:110007668-110008400 | Common:3; Rare:233 | ||||
| chr10:110008582-110008922 | Common:6; Rare:95 | ||||
| chr10:110225855-110226281 | Common:2; Rare:120 | ||||
| chr10:110304890-110305049 | Common:2; Rare:58 | ||||
| chr10:110567381-110567787 | Common:2; Rare:119; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110871737-110871964 | Rare:70 |