| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216109050-216109442 | Common:8; Rare:108 | ||||
| chr2:216412460-216412733 | Common:3; Rare:52; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:216498653-216498993 | Common:12; Rare:133 | ||||
| chr2:218216919-218217282 | Common:3; Rare:112 | ||||
| chr2:218217582-218217844 | Common:2; Rare:58 | ||||
| chr2:218270044-218270349 | Common:5; Rare:96 | ||||
| chr2:218286744-218287013 | Common:1; Rare:50 | ||||
| chr2:218287296-218287421 | Common:1; Rare:20 | ||||
| chr2:218292467-218292604 | Rare:35 | ||||
| chr2:218322951-218323334 | Common:7; Rare:128 | ||||
| chr2:218397998-218398339 | Common:1; Rare:129 | ||||
| chr2:218398524-218398664 | Common:1; Rare:49 | ||||
| chr2:218399431-218399888 | Common:1; Rare:204 | ||||
| chr2:218400287-218400317 | Rare:12 | ||||
| chr2:218400412-218400752 | Common:7; Rare:125 |