| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233387708-233387938 | Common:1; Rare:57 | ||||
| chr2:233387951-233388298 | Common:1; Rare:99 | ||||
| chr2:233854426-233854867 | Common:6; Rare:117 | ||||
| chr2:236167320-236167498 | Common:3; Rare:72 | ||||
| chr2:237085742-237085955 | Common:2; Rare:77 | ||||
| chr2:237485184-237485466 | Common:1; Rare:43 | ||||
| chr2:237486322-237486420 | Rare:21 | ||||
| chr2:237487079-237487346 | Common:3; Rare:70 | ||||
| chr2:238060706-238061156 | Common:6; Rare:143 | ||||
| chr2:238203583-238203821 | Common:3; Rare:101 | ||||
| chr2:238290133-238290470 | Common:2; Rare:78 | ||||
| chr2:238426647-238427073 | Common:6; Rare:126 | ||||
| chr2:238848086-238848336 | Rare:61 | ||||
| chr2:239401641-239401805 | Rare:86 | ||||
| chr2:240025225-240025441 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 |