| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231460160-231460869 | Common:4; Rare:306 | ||||
| chr2:231464337-231464807 | Common:3; Rare:164 | ||||
| chr2:231781255-231781426 | Rare:43 | ||||
| chr2:231961671-231961756 | Rare:21; Clinvar:1 | ||||
| chr2:232550545-232550740 | Rare:82 | ||||
| chr2:237085761-237085955 | Common:2; Rare:72 | ||||
| chr2:237413954-237414302 | Common:2; Rare:69; Clinvar (benign):3 | ||||
| chr2:237487136-237487298 | Common:3; Rare:44 | ||||
| chr2:237627500-237627669 | Common:2; Rare:60 | ||||
| chr2:238060748-238061112 | Common:6; Rare:116 | ||||
| chr2:238426892-238427065 | Common:1; Rare:62 | ||||
| chr2:238847884-238848106 | Common:1; Rare:47 | ||||
| chr2:239401641-239401720 | Rare:30 | ||||
| chr2:240025227-240025477 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560766-240560825 | Rare:24 |