| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:103396386-103396743 | Rare:123 | ||||
| chr10:103458898-103459173 | Common:1; Rare:47 | ||||
| chr10:103967018-103967295 | Common:1; Rare:79 | ||||
| chr10:103967544-103967869 | Rare:92 | ||||
| chr10:104231818-104231892 | Common:1; Rare:13 | ||||
| chr10:104268878-104269193 | Common:3; Rare:75 | ||||
| chr10:104338393-104338567 | Rare:45 | ||||
| chr10:104338631-104338756 | Rare:25 | ||||
| chr10:109877725-109878019 | Common:3; Rare:83 | ||||
| chr10:109923406-109923660 | Common:2; Rare:93 | ||||
| chr10:110006037-110006084 | Rare:11 | ||||
| chr10:110007678-110008292 | Common:2; Rare:201 | ||||
| chr10:110304849-110305214 | Common:2; Rare:118 | ||||
| chr10:110497730-110497955 | Common:5; Rare:80 | ||||
| chr10:110567401-110567811 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):5 |