| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216694591-216694833 | Rare:65 | ||||
| chr2:218217107-218217420 | Common:2; Rare:101 | ||||
| chr2:218217735-218217880 | Common:1; Rare:39 | ||||
| chr2:218270037-218270538 | Common:5; Rare:161; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218289992-218290219 | Common:3; Rare:38 | ||||
| chr2:218322986-218323248 | Common:5; Rare:79 | ||||
| chr2:218568269-218568632 | Common:3; Rare:98 | ||||
| chr2:218568733-218568966 | Common:1; Rare:65 | ||||
| chr2:218659339-218659379 | Common:1; Rare:9 | ||||
| chr2:218659565-218659811 | Common:1; Rare:66 | ||||
| chr2:218671975-218672334 | Common:2; Rare:89 | ||||
| chr2:218745792-218746163 | Common:1; Rare:71 | ||||
| chr2:219176253-219176555 | Common:3; Rare:83 | ||||
| chr2:219176897-219177120 | Common:4; Rare:67 | ||||
| chr2:219177819-219177933 | Common:3; Rare:24 |