| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:103918120-103918423 | Common:4; Rare:84 | ||||
| chr10:103967023-103967043 | Rare:2 | ||||
| chr10:104268695-104269202 | Common:7; Rare:109 | ||||
| chr10:104328894-104328983 | Rare:14 | ||||
| chr10:104328986-104329047 | Rare:17 | ||||
| chr10:107164097-107164142 | Rare:13 | ||||
| chr10:109923423-109923655 | Common:2; Rare:89 | ||||
| chr10:110007731-110008269 | Common:2; Rare:167 | ||||
| chr10:110225904-110226249 | Common:2; Rare:93 | ||||
| chr10:110304870-110304982 | Common:2; Rare:47 | ||||
| chr10:110567404-110567825 | Common:2; Rare:127; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110871627-110871964 | Rare:109 | ||||
| chr10:110918923-110918945 | Rare:6 | ||||
| chr10:110919122-110919321 | Common:1; Rare:48 | ||||
| chr10:110919327-110919645 | Common:7; Rare:88; Clinvar:1 |