| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144264710-144265480 | Common:5; Rare:274 | ||||
| chr8:144291345-144291679 | Common:2; Rare:209 | ||||
| chr8:144326647-144327077 | Common:4; Rare:187 | ||||
| chr8:144359224-144359989 | Common:4; Rare:646; Clinvar:26; Clinvar (benign):18; Clinvar (pathogenic):14 | ||||
| chr8:144373788-144374113 | Common:8; Rare:191 | ||||
| chr8:144409221-144409451 | Rare:142 | ||||
| chr8:144413545-144413719 | Rare:99; Clinvar:2 | ||||
| chr8:144416417-144416889 | Common:10; Rare:316; Clinvar:5; Clinvar (benign):10 | ||||
| chr8:144427680-144427990 | Common:4; Rare:164 | ||||
| chr8:144428480-144428673 | Common:4; Rare:131 | ||||
| chr8:144444364-144444652 | Common:2; Rare:173 | ||||
| chr8:144462849-144463047 | Rare:94 | ||||
| chr8:144465342-144465505 | Common:6; Rare:120 | ||||
| chr8:144465640-144466200 | Common:2; Rare:167 | ||||
| chr8:144477831-144478128 | Common:12; Rare:200 |