| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144147788-144148058 | Common:2; Rare:63 | ||||
| chr8:144291348-144291668 | Common:1; Rare:104 | ||||
| chr8:144359416-144359759 | Common:1; Rare:113; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr8:144373781-144374076 | Common:3; Rare:96 | ||||
| chr8:144413530-144413719 | Rare:60; Clinvar:1 | ||||
| chr8:144428461-144428673 | Common:2; Rare:84 | ||||
| chr8:144462861-144463052 | Rare:90 | ||||
| chr8:144477871-144478104 | Common:5; Rare:86 | ||||
| chr8:144517668-144518014 | Common:1; Rare:118; Clinvar:10; Clinvar (benign):2 | ||||
| chr8:144755420-144755663 | Common:1; Rare:91 | ||||
| chr8:144787279-144787455 | Common:2; Rare:56 | ||||
| chr8:144792265-144792592 | Common:3; Rare:120 | ||||
| chr8:144827259-144827617 | Common:2; Rare:95 | ||||
| chr8:144901409-144901600 | Common:1; Rare:56 | ||||
| chr8:144950593-144950908 | Common:4; Rare:99 |