| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58549996-58550284 | Common:2; Rare:106 | ||||
| chr19:58554195-58554571 | Rare:98 | ||||
| chr19:58554910-58555219 | Common:2; Rare:98 | ||||
| chr19:58558260-58558692 | Rare:131 | ||||
| chr19:58558884-58559126 | Common:1; Rare:77 | ||||
| chr19:58573286-58573614 | Common:1; Rare:85 | ||||
| chr2:676306-676483 | Common:3; Rare:39 | ||||
| chr2:677352-677564 | Common:1; Rare:90 | ||||
| chr2:3377785-3378028 | Common:2; Rare:70 | ||||
| chr2:3379594-3379808 | Common:2; Rare:85 | ||||
| chr2:3519465-3519660 | Common:2; Rare:60 | ||||
| chr2:3558136-3558740 | Common:6; Rare:213 | ||||
| chr2:3575091-3575447 | Common:2; Rare:99; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:3605239-3605600 | Common:8; Rare:38 | ||||
| chr2:9003957-9004087 | Rare:55 |