| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:77926447-77926629 | Common:2; Rare:47 | ||||
| chr10:77926687-77926974 | Common:2; Rare:99 | ||||
| chr10:78029470-78029967 | Common:5; Rare:110; Clinvar (benign):1 | ||||
| chr10:78033610-78034316 | Common:7; Rare:229; Clinvar (benign):4 | ||||
| chr10:79068736-79069102 | Common:3; Rare:113 | ||||
| chr10:79069193-79069269 | Common:1; Rare:22 | ||||
| chr10:79069512-79069648 | Common:3; Rare:31 | ||||
| chr10:79347335-79347642 | Common:4; Rare:80 | ||||
| chr10:79347926-79348056 | Rare:22 | ||||
| chr10:79348066-79348262 | Common:1; Rare:47 | ||||
| chr10:79444855-79445255 | Common:1; Rare:81 | ||||
| chr10:79445306-79445412 | Rare:26 | ||||
| chr10:79445414-79446027 | Common:2; Rare:172 | ||||
| chr10:79982124-79982231 | Common:2; Rare:24 | ||||
| chr10:80078550-80078833 | Rare:108 |