| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216108851-216109591 | Common:27; Rare:401 | ||||
| chr2:216412654-216412827 | Rare:34 | ||||
| chr2:216498677-216498949 | Common:16; Rare:221 | ||||
| chr2:216499117-216499369 | Common:3; Rare:95 | ||||
| chr2:217901881-217902118 | Common:4; Rare:54 | ||||
| chr2:217903930-217904340 | Common:2; Rare:136 | ||||
| chr2:218217017-218217229 | Common:2; Rare:131 | ||||
| chr2:218245270-218245650 | Rare:100 | ||||
| chr2:218269596-218270012 | Common:1; Rare:176 | ||||
| chr2:218270060-218270565 | Common:10; Rare:292; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:218287260-218287460 | Common:1; Rare:34 | ||||
| chr2:218292468-218292643 | Common:1; Rare:93 | ||||
| chr2:218316470-218316930 | Common:4; Rare:87 | ||||
| chr2:218322978-218323361 | Common:12; Rare:239 | ||||
| chr2:218389251-218390060 | Common:2; Rare:281 |