| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237487141-237487359 | Common:3; Rare:57 | ||||
| chr2:237540527-237540810 | Common:2; Rare:79 | ||||
| chr2:237966704-237967039 | Common:4; Rare:100 | ||||
| chr2:238060734-238061148 | Common:6; Rare:128 | ||||
| chr2:238203543-238203804 | Common:5; Rare:100 | ||||
| chr2:238426620-238426714 | Common:1; Rare:18 | ||||
| chr2:239401641-239401750 | Rare:52 | ||||
| chr2:240025248-240025455 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136234-240136432 | Common:1; Rare:90 | ||||
| chr2:240560724-240560873 | Common:1; Rare:70 | ||||
| chr2:240561027-240561258 | Common:2; Rare:99 | ||||
| chr2:241102263-241102508 | Common:2; Rare:76 | ||||
| chr2:241149439-241149549 | Common:1; Rare:33 | ||||
| chr2:241188394-241188765 | Common:2; Rare:95 | ||||
| chr2:241230858-241231097 | Common:1; Rare:59 |