| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:154407025-154407695 | Common:9; Rare:216 | ||||
| chr1:154408337-154408737 | Common:3; Rare:80 | ||||
| chr1:154410753-154411153 | Common:2; Rare:72 | ||||
| chr1:154411487-154411887 | Common:1; Rare:95 | ||||
| chr1:154413044-154413570 | Rare:169 | ||||
| chr1:154416558-154416958 | Common:2; Rare:119 | ||||
| chr1:154419170-154419430 | Common:2; Rare:42 | ||||
| chr1:154420350-154420650 | Common:2; Rare:62 | ||||
| chr1:154435551-154435992 | Common:6; Rare:128 | ||||
| chr1:154466900-154467300 | Common:1; Rare:117 | ||||
| chr1:154492201-154492422 | Common:1; Rare:44 | ||||
| chr1:154492469-154492869 | Common:2; Rare:112 | ||||
| chr1:154559591-154559751 | Rare:26 | ||||
| chr1:154598502-154599619 | Common:9; Rare:344; Clinvar (pathogenic):1 | ||||
| chr1:154606543-154606943 | Common:1; Rare:93 |