| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69436906-69437223 | Common:1; Rare:81 | ||||
| chr2:69437322-69437506 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):5 | ||||
| chr2:69437510-69437724 | Common:1; Rare:96; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:69643180-69643356 | Rare:40 | ||||
| chr2:69643586-69643955 | Rare:118 | ||||
| chr2:69643974-69644276 | Common:7; Rare:53 | ||||
| chr2:69644409-69644560 | Common:2; Rare:31 | ||||
| chr2:69741263-69741623 | Common:1; Rare:67 | ||||
| chr2:69741686-69742188 | Common:4; Rare:102 | ||||
| chr2:69781500-69781698 | Rare:57 | ||||
| chr2:69829213-69829353 | Common:2; Rare:28 | ||||
| chr2:69829413-69829739 | Common:1; Rare:122 | ||||
| chr2:69893850-69894021 | Rare:46 | ||||
| chr2:69914475-69915188 | Common:2; Rare:177 | ||||
| chr2:70086763-70087158 | Common:3; Rare:170 |