| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144104111-144104542 | Common:4; Rare:157 | ||||
| chr8:144137614-144137774 | Common:1; Rare:39 | ||||
| chr8:144326850-144327043 | Common:1; Rare:52 | ||||
| chr8:144409259-144409579 | Common:1; Rare:101 | ||||
| chr8:144427734-144427967 | Common:1; Rare:63 | ||||
| chr8:144428492-144428638 | Common:2; Rare:53 | ||||
| chr8:144465356-144465587 | Common:4; Rare:80 | ||||
| chr8:144475759-144476026 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:144477857-144478102 | Common:5; Rare:92 | ||||
| chr8:144500756-144501191 | Rare:213 | ||||
| chr8:144503281-144503597 | Common:2; Rare:77 | ||||
| chr8:144517675-144518023 | Common:1; Rare:121; Clinvar:10; Clinvar (benign):2 | ||||
| chr8:144755421-144755684 | Common:1; Rare:99 | ||||
| chr8:144792335-144792594 | Common:3; Rare:104 | ||||
| chr8:144827248-144827608 | Common:1; Rare:95 |