| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208265928-208266296 | Common:9; Rare:124; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423748-209424081 | Common:2; Rare:98 | ||||
| chr2:209579452-209579468 | Rare:1 | ||||
| chr2:209579570-209579676 | Common:1; Rare:22 | ||||
| chr2:210002488-210002670 | Common:5; Rare:63 | ||||
| chr2:210477536-210477686 | Rare:43 | ||||
| chr2:215311879-215312137 | Common:8; Rare:100 | ||||
| chr2:215436022-215436287 | Common:2; Rare:84 | ||||
| chr2:216081753-216081925 | Common:1; Rare:62 | ||||
| chr2:216498754-216498977 | Common:7; Rare:96 | ||||
| chr2:218217019-218217212 | Common:1; Rare:65 | ||||
| chr2:218270095-218270574 | Common:5; Rare:153; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218322978-218323275 | Common:6; Rare:97 | ||||
| chr2:218568229-218568702 | Common:5; Rare:118 | ||||
| chr2:218568731-218568962 | Common:1; Rare:65 |