| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144291398-144291651 | Rare:82 | ||||
| chr8:144292540-144292675 | Rare:32 | ||||
| chr8:144326658-144327092 | Common:3; Rare:128 | ||||
| chr8:144358445-144358623 | Common:1; Rare:79 | ||||
| chr8:144358902-144359810 | Common:7; Rare:388; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
| chr8:144373813-144374102 | Common:4; Rare:96 | ||||
| chr8:144409288-144409479 | Rare:63 | ||||
| chr8:144409650-144410080 | Common:4; Rare:122 | ||||
| chr8:144428497-144428734 | Common:3; Rare:89 | ||||
| chr8:144444403-144444663 | Common:1; Rare:84 | ||||
| chr8:144462802-144463086 | Rare:144 | ||||
| chr8:144466455-144467095 | Common:11; Rare:393 | ||||
| chr8:144477871-144478072 | Common:5; Rare:78 | ||||
| chr8:144499048-144499448 | Common:2; Rare:173 | ||||
| chr8:144508623-144508798 | Common:2; Rare:53 |