| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143878440-143878581 | Common:4; Rare:43 | ||||
| chr8:143939352-143939387 | Rare:10 | ||||
| chr8:143939491-143939729 | Common:3; Rare:76 | ||||
| chr8:143943901-143944112 | Rare:83 | ||||
| chr8:143986394-143986481 | Rare:14 | ||||
| chr8:144060665-144060820 | Rare:45 | ||||
| chr8:144078539-144078874 | Common:1; Rare:110 | ||||
| chr8:144082538-144082689 | Common:1; Rare:54 | ||||
| chr8:144096101-144096419 | Common:1; Rare:122; Clinvar (benign):3 | ||||
| chr8:144103673-144103881 | Common:1; Rare:72 | ||||
| chr8:144104163-144104526 | Common:3; Rare:123 | ||||
| chr8:144104693-144105069 | Common:2; Rare:119 | ||||
| chr8:144291336-144291673 | Common:1; Rare:110 | ||||
| chr8:144308945-144309084 | Rare:34 | ||||
| chr8:144413518-144413704 | Rare:64; Clinvar:1 |