| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144095936-144096610 | Common:3; Rare:322; Clinvar:2; Clinvar (benign):7 | ||||
| chr8:144103678-144103881 | Common:2; Rare:129 | ||||
| chr8:144104089-144104599 | Common:8; Rare:345 | ||||
| chr8:144104858-144105033 | Common:2; Rare:105 | ||||
| chr8:144137600-144137850 | Common:4; Rare:135 | ||||
| chr8:144147762-144148079 | Common:3; Rare:148 | ||||
| chr8:144291344-144291651 | Common:2; Rare:198 | ||||
| chr8:144326632-144327074 | Common:6; Rare:251 | ||||
| chr8:144372794-144373094 | Common:18; Rare:129 | ||||
| chr8:144373768-144374097 | Common:7; Rare:190 | ||||
| chr8:144400227-144401201 | Common:1; Rare:723 | ||||
| chr8:144409127-144409580 | Common:1; Rare:244 | ||||
| chr8:144416447-144416698 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):4 | ||||
| chr8:144416774-144417004 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:144428393-144428747 | Common:6; Rare:227 |