| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219495888-219496188 | Common:1; Rare:54 | ||||
| chr2:219498691-219498928 | Common:2; Rare:50 | ||||
| chr2:226799176-226799331 | Common:1; Rare:38 | ||||
| chr2:227325184-227325341 | Common:4; Rare:56 | ||||
| chr2:229921918-229922161 | Common:3; Rare:96 | ||||
| chr2:229922207-229922506 | Common:1; Rare:90 | ||||
| chr2:231464376-231464769 | Common:3; Rare:134 | ||||
| chr2:231961654-231961747 | Rare:25; Clinvar:1 | ||||
| chr2:232525894-232526247 | Common:3; Rare:117; Clinvar (benign):1 | ||||
| chr2:232550552-232550736 | Rare:74 | ||||
| chr2:233854516-233854720 | Common:4; Rare:50 | ||||
| chr2:236264352-236264470 | Rare:25 | ||||
| chr2:237085761-237085955 | Common:2; Rare:72 | ||||
| chr2:237627320-237627702 | Common:3; Rare:118 | ||||
| chr2:240025291-240025443 | Common:1; Rare:61; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 |