| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144060678-144060855 | Rare:56 | ||||
| chr8:144078532-144078740 | Common:1; Rare:63 | ||||
| chr8:144082490-144082682 | Common:2; Rare:65 | ||||
| chr8:144104156-144104492 | Common:3; Rare:104 | ||||
| chr8:144137614-144137774 | Common:1; Rare:39 | ||||
| chr8:144264738-144264966 | Common:1; Rare:48 | ||||
| chr8:144373788-144374080 | Common:3; Rare:94 | ||||
| chr8:144409239-144409537 | Common:1; Rare:97 | ||||
| chr8:144413525-144413735 | Common:1; Rare:67; Clinvar:1 | ||||
| chr8:144428446-144428638 | Common:2; Rare:75 | ||||
| chr8:144477891-144478104 | Common:4; Rare:78 | ||||
| chr8:144508959-144509099 | Rare:38 | ||||
| chr8:144517701-144518017 | Common:1; Rare:109; Clinvar:10; Clinvar (benign):2 | ||||
| chr8:144528938-144529208 | Common:2; Rare:112 | ||||
| chr8:144755461-144755729 | Common:1; Rare:90 |