| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208025456-208025633 | Common:2; Rare:44 | ||||
| chr2:208189912-208190328 | Common:1; Rare:98 | ||||
| chr2:208254234-208254504 | Rare:69 | ||||
| chr2:208254999-208255266 | Common:2; Rare:70 | ||||
| chr2:208255437-208255543 | Common:2; Rare:18 | ||||
| chr2:208265534-208265850 | Common:1; Rare:55 | ||||
| chr2:208265884-208266360 | Common:9; Rare:152; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423777-209424078 | Common:1; Rare:91 | ||||
| chr2:209579222-209579499 | Common:8; Rare:53 | ||||
| chr2:209661328-209661571 | Common:2; Rare:41 | ||||
| chr2:209772268-209772504 | Common:1; Rare:36 | ||||
| chr2:209960762-209960952 | Rare:36 | ||||
| chr2:210002414-210002645 | Common:6; Rare:77 | ||||
| chr2:210170631-210170935 | Common:2; Rare:110 | ||||
| chr2:210171345-210171581 | Common:4; Rare:88 |