| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:209579646-209579693 | Common:1; Rare:5 | ||||
| chr2:209771728-209772038 | Common:2; Rare:87 | ||||
| chr2:213284238-213284497 | Rare:85 | ||||
| chr2:215311912-215312126 | Common:7; Rare:88 | ||||
| chr2:215370302-215370590 | Common:10; Rare:91 | ||||
| chr2:215435831-215435904 | Rare:13 | ||||
| chr2:215436044-215436356 | Common:2; Rare:98 | ||||
| chr2:216081761-216081945 | Common:1; Rare:63 | ||||
| chr2:216498754-216498876 | Common:3; Rare:50 | ||||
| chr2:216694444-216694484 | Rare:7 | ||||
| chr2:216694488-216694719 | Rare:57 | ||||
| chr2:216694723-216695010 | Rare:59 | ||||
| chr2:218270089-218270534 | Common:5; Rare:137; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218292496-218292815 | Common:1; Rare:70 | ||||
| chr2:218568290-218568667 | Common:4; Rare:98 |