| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:102619408-102619769 | Common:2; Rare:87 | ||||
| chr2:102736871-102736944 | Common:1; Rare:21 | ||||
| chr2:105037884-105038106 | Common:3; Rare:78 | ||||
| chr2:105337463-105337612 | Common:1; Rare:72 | ||||
| chr2:105398965-105399249 | Common:1; Rare:103 | ||||
| chr2:106194237-106194543 | Common:6; Rare:129 | ||||
| chr2:108534163-108534483 | Common:7; Rare:131 | ||||
| chr2:108719372-108719577 | Common:3; Rare:84; Clinvar (benign):2 | ||||
| chr2:109613875-109614031 | Common:2; Rare:52 | ||||
| chr2:110678004-110678267 | Rare:89 | ||||
| chr2:110732407-110732641 | Rare:80 | ||||
| chr2:111122443-111122844 | Common:3; Rare:155 | ||||
| chr2:111884087-111884283 | Common:2; Rare:58 | ||||
| chr2:112055474-112055587 | Common:2; Rare:29 | ||||
| chr2:112275399-112275642 | Common:1; Rare:81 |