| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178480154-178480366 | Common:1; Rare:67 | ||||
| chr2:179264502-179264857 | Common:4; Rare:131 | ||||
| chr2:180007040-180007424 | Common:1; Rare:98 | ||||
| chr2:180983919-180984081 | Rare:45 | ||||
| chr2:181457230-181457565 | Common:2; Rare:124 | ||||
| chr2:181656858-181657015 | Rare:75; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:181657087-181657207 | Rare:28 | ||||
| chr2:181680504-181680733 | Rare:52; Clinvar:1 | ||||
| chr2:181891623-181892090 | Common:4; Rare:196 | ||||
| chr2:182716119-182716461 | Common:2; Rare:112 | ||||
| chr2:182866548-182866765 | Common:1; Rare:51 | ||||
| chr2:182867121-182867223 | Rare:26 | ||||
| chr2:183078658-183078797 | Rare:29 | ||||
| chr2:183124230-183124484 | Common:4; Rare:85 | ||||
| chr2:184598343-184598605 | Common:2; Rare:80 |