| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144395887-144396066 | Common:1; Rare:39 | ||||
| chr8:144409342-144409676 | Common:1; Rare:110 | ||||
| chr8:144413502-144413712 | Rare:72; Clinvar:1 | ||||
| chr8:144428487-144428636 | Common:2; Rare:55 | ||||
| chr8:144465356-144465492 | Common:3; Rare:53 | ||||
| chr8:144477902-144478082 | Common:4; Rare:69 | ||||
| chr8:144500952-144501226 | Rare:131 | ||||
| chr8:144508946-144509099 | Rare:42 | ||||
| chr8:144509811-144509841 | Rare:21 | ||||
| chr8:144511777-144511904 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr8:144755440-144755684 | Common:1; Rare:87 | ||||
| chr8:144792348-144792553 | Common:2; Rare:80 | ||||
| chr8:144827259-144827604 | Common:1; Rare:91 | ||||
| chr8:144852982-144853137 | Rare:57 | ||||
| chr8:144950817-144950912 | Common:1; Rare:33 |