| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231710278-231710518 | Common:2; Rare:120 | ||||
| chr2:231781246-231781462 | Rare:63 | ||||
| chr2:231961648-231961739 | Rare:24; Clinvar:1 | ||||
| chr2:232550555-232550723 | Rare:64 | ||||
| chr2:232550977-232551110 | Rare:25 | ||||
| chr2:233854493-233854775 | Common:4; Rare:81 | ||||
| chr2:236167313-236167477 | Common:3; Rare:70 | ||||
| chr2:236507450-236507653 | Common:6; Rare:69 | ||||
| chr2:237085769-237085946 | Common:2; Rare:61 | ||||
| chr2:238060738-238061099 | Common:6; Rare:112 | ||||
| chr2:238203616-238203815 | Common:3; Rare:85 | ||||
| chr2:240025276-240025480 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136259-240136382 | Rare:47 | ||||
| chr2:240560766-240560894 | Common:2; Rare:59 | ||||
| chr2:241102280-241102375 | Common:2; Rare:34 |