| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:69124508-69124561 | Common:1; Rare:13 | ||||
| chr10:69179863-69180342 | Common:3; Rare:158 | ||||
| chr10:69318203-69318407 | Common:1; Rare:43 | ||||
| chr10:69318602-69318954 | Common:4; Rare:104 | ||||
| chr10:69319479-69319579 | Common:1; Rare:17 | ||||
| chr10:69408651-69409112 | Common:19; Rare:143 | ||||
| chr10:70132537-70133012 | Common:2; Rare:123 | ||||
| chr10:70133037-70133148 | Common:3; Rare:37 | ||||
| chr10:70145983-70146112 | Rare:41 | ||||
| chr10:70146128-70146278 | Common:2; Rare:57 | ||||
| chr10:70146493-70146944 | Common:1; Rare:121 | ||||
| chr10:70170453-70170830 | Common:3; Rare:104 | ||||
| chr10:70233298-70233803 | Common:6; Rare:155; Clinvar (benign):1 | ||||
| chr10:70381899-70382099 | Common:1; Rare:43 | ||||
| chr10:70382530-70382896 | Common:5; Rare:137 |