| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102419103-102419239 | Rare:30 | ||||
| chr10:102419666-102419838 | Rare:50 | ||||
| chr10:102461075-102461428 | Common:1; Rare:79 | ||||
| chr10:102502633-102503072 | Common:1; Rare:114 | ||||
| chr10:102714197-102714489 | Common:2; Rare:104 | ||||
| chr10:102776078-102776215 | Common:1; Rare:20 | ||||
| chr10:102854155-102854284 | Common:1; Rare:45 | ||||
| chr10:103276940-103277163 | Common:1; Rare:57 | ||||
| chr10:103351038-103351151 | Rare:44 | ||||
| chr10:103396397-103396710 | Rare:112 | ||||
| chr10:104121867-104122174 | Common:2; Rare:101 | ||||
| chr10:104268935-104269184 | Common:3; Rare:56 | ||||
| chr10:109923425-109923640 | Common:2; Rare:79 | ||||
| chr10:110005894-110006106 | Common:4; Rare:60 | ||||
| chr10:110567631-110567781 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):5 |