| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:69124498-69124652 | Common:1; Rare:41 | ||||
| chr10:69179859-69180355 | Common:4; Rare:167 | ||||
| chr10:69318055-69318362 | Common:3; Rare:77 | ||||
| chr10:69318407-69318510 | Rare:25 | ||||
| chr10:69318535-69319125 | Common:5; Rare:154 | ||||
| chr10:69319477-69319579 | Common:1; Rare:18 | ||||
| chr10:69408663-69409113 | Common:19; Rare:138 | ||||
| chr10:70132504-70133032 | Common:3; Rare:132 | ||||
| chr10:70146043-70146283 | Common:2; Rare:88 | ||||
| chr10:70146565-70146936 | Common:1; Rare:98 | ||||
| chr10:70170446-70170871 | Common:3; Rare:113 | ||||
| chr10:70233105-70233115 | Rare:4 | ||||
| chr10:70233245-70233804 | Common:6; Rare:167; Clinvar (benign):1 | ||||
| chr10:70381899-70382185 | Common:1; Rare:65 | ||||
| chr10:70382497-70382893 | Common:5; Rare:150 |