| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144096064-144096154 | Rare:35 | ||||
| chr8:144104159-144104499 | Common:3; Rare:106 | ||||
| chr8:144409342-144409644 | Common:1; Rare:101 | ||||
| chr8:144413552-144413729 | Common:1; Rare:51; Clinvar:1 | ||||
| chr8:144416826-144417137 | Common:1; Rare:73 | ||||
| chr8:144428489-144428638 | Common:2; Rare:55 | ||||
| chr8:144477887-144478089 | Common:4; Rare:80 | ||||
| chr8:144500944-144501192 | Rare:121 | ||||
| chr8:144755461-144755680 | Common:1; Rare:74 | ||||
| chr8:144792335-144792590 | Common:3; Rare:102 | ||||
| chr8:144798669-144798922 | Common:3; Rare:83 | ||||
| chr8:144827234-144827603 | Common:2; Rare:94 | ||||
| chr8:145052153-145052504 | Common:11; Rare:91 | ||||
| chr9:178912-179246 | Common:8; Rare:73 | ||||
| chr9:214625-214869 | Common:5; Rare:138; Clinvar (benign):1 |