| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144397564-144397878 | Common:1; Rare:130 | ||||
| chr8:144398564-144398817 | Common:1; Rare:110 | ||||
| chr8:144415028-144415356 | Rare:148; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr8:144417849-144418127 | Rare:68 | ||||
| chr8:144429392-144429429 | Common:1; Rare:5 | ||||
| chr8:144430463-144430822 | Common:2; Rare:87 | ||||
| chr8:144440171-144440396 | Common:3; Rare:69 | ||||
| chr8:144502000-144502288 | Common:1; Rare:76 | ||||
| chr8:144506587-144506775 | Common:4; Rare:119 | ||||
| chr8:144507964-144508289 | Common:1; Rare:76 | ||||
| chr8:145002835-145003055 | Common:2; Rare:76 | ||||
| chr9:503814-504134 | Common:5; Rare:81 | ||||
| chr9:4531721-4531916 | Common:1; Rare:60 | ||||
| chr9:4532449-4532589 | Rare:39 | ||||
| chr9:4561394-4561504 | Common:2; Rare:46; Clinvar:1 |