| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:230995993-230996152 | Common:3; Rare:23 | ||||
| chr2:231198556-231198661 | Common:1; Rare:35 | ||||
| chr2:231464150-231464197 | Rare:16 | ||||
| chr2:231464311-231464792 | Common:3; Rare:162 | ||||
| chr2:231707005-231707180 | Rare:40 | ||||
| chr2:231710314-231710551 | Common:2; Rare:117 | ||||
| chr2:231781247-231781465 | Rare:65 | ||||
| chr2:231781607-231781741 | Common:1; Rare:40 | ||||
| chr2:231786187-231786463 | Common:3; Rare:76 | ||||
| chr2:231961626-231961748 | Rare:39; Clinvar:2 | ||||
| chr2:232550545-232550739 | Rare:81 | ||||
| chr2:232776551-232776598 | Rare:8 | ||||
| chr2:233060273-233060375 | Rare:16 | ||||
| chr2:233251510-233251833 | Common:3; Rare:107 | ||||
| chr2:233854516-233854752 | Common:4; Rare:61 |