| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:240870402-240870708 | Common:1; Rare:86; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr2:240871162-240871443 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr2:240876508-240876648 | Rare:24 | ||||
| chr2:241102276-241102517 | Common:2; Rare:70 | ||||
| chr2:241149439-241149614 | Common:1; Rare:57 | ||||
| chr2:241230912-241231182 | Common:1; Rare:63 | ||||
| chr2:241255049-241255242 | Common:1; Rare:48 | ||||
| chr2:241272769-241272980 | Rare:76 | ||||
| chr2:241315121-241315428 | Common:5; Rare:102 | ||||
| chr2:241315619-241316195 | Common:5; Rare:210 | ||||
| chr2:241508539-241508855 | Common:2; Rare:96 | ||||
| chr2:241637042-241637204 | Rare:66 | ||||
| chr2:241637550-241637704 | Common:1; Rare:81 | ||||
| chr2:241686709-241687118 | Common:4; Rare:130 | ||||
| chr2:241701877-241702064 | Common:1; Rare:77 |