| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:208244078-208244147 | Rare:8 | ||||
| chr1:208244198-208244532 | Common:2; Rare:89 | ||||
| chr1:209652369-209652610 | Common:3; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:209675268-209675924 | Common:4; Rare:179 | ||||
| chr1:209755751-209756064 | Common:1; Rare:62 | ||||
| chr1:209784537-209784698 | Rare:49 | ||||
| chr1:209806008-209806299 | Common:5; Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:210232800-210232955 | Common:1; Rare:45 | ||||
| chr1:210328868-210329004 | Rare:45 | ||||
| chr1:211259048-211259400 | Common:1; Rare:110 | ||||
| chr1:211259458-211259587 | Common:1; Rare:54 | ||||
| chr1:211675589-211675809 | Common:1; Rare:44 | ||||
| chr1:212035490-212035793 | Common:2; Rare:82 | ||||
| chr1:212285042-212285449 | Common:4; Rare:133 | ||||
| chr1:212285756-212286147 | Common:2; Rare:108 |