| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144428479-144428642 | Common:2; Rare:62 | ||||
| chr8:144444376-144444606 | Common:1; Rare:73 | ||||
| chr8:144466857-144466972 | Common:3; Rare:62 | ||||
| chr8:144468353-144468593 | Common:4; Rare:106 | ||||
| chr8:144477901-144478109 | Common:4; Rare:76 | ||||
| chr8:144508998-144509106 | Rare:32 | ||||
| chr8:144509785-144510015 | Rare:106 | ||||
| chr8:144517742-144518039 | Common:1; Rare:105; Clinvar:8; Clinvar (benign):1 | ||||
| chr8:144528915-144529202 | Common:2; Rare:122 | ||||
| chr8:144792299-144792585 | Common:3; Rare:109 | ||||
| chr8:144827209-144827609 | Common:2; Rare:112 | ||||
| chr8:144853478-144853570 | Common:1; Rare:25 | ||||
| chr8:144901386-144901727 | Common:1; Rare:96 | ||||
| chr8:145052182-145052518 | Common:10; Rare:95 | ||||
| chr9:706959-707206 | Common:4; Rare:82 |