| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69387121-69387417 | Rare:170; Clinvar:4 | ||||
| chr2:69437391-69437707 | Common:1; Rare:187; Clinvar:7; Clinvar (benign):5 | ||||
| chr2:69643090-69643510 | Common:3; Rare:129 | ||||
| chr2:69643563-69643889 | Rare:195 | ||||
| chr2:69741741-69742192 | Common:8; Rare:176 | ||||
| chr2:69829477-69829813 | Common:2; Rare:214 | ||||
| chr2:69893869-69894025 | Rare:79 | ||||
| chr2:69914448-69915371 | Common:10; Rare:710 | ||||
| chr2:70086897-70087143 | Common:2; Rare:234 | ||||
| chr2:70087286-70087852 | Common:5; Rare:374 | ||||
| chr2:70190658-70190785 | Rare:36 | ||||
| chr2:70190899-70191134 | Common:2; Rare:96 | ||||
| chr2:70248441-70248812 | Common:10; Rare:271 | ||||
| chr2:70257973-70258213 | Common:2; Rare:85 | ||||
| chr2:70293190-70293590 | Common:2; Rare:178 |