| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74178800-74179012 | Common:2; Rare:60 | ||||
| chr2:74374558-74374803 | Rare:58 | ||||
| chr2:74385192-74385545 | Common:2; Rare:47 | ||||
| chr2:74391792-74392147 | Common:2; Rare:166 | ||||
| chr2:74421579-74421793 | Rare:73 | ||||
| chr2:74458113-74458510 | Common:1; Rare:123 | ||||
| chr2:74465354-74465455 | Common:1; Rare:27 | ||||
| chr2:74482757-74483119 | Common:1; Rare:129 | ||||
| chr2:74507653-74507795 | Rare:30 | ||||
| chr2:74529639-74529872 | Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74555624-74555810 | Common:1; Rare:53 | ||||
| chr2:74654106-74654382 | Common:1; Rare:95 | ||||
| chr2:74958530-74958727 | Common:4; Rare:79 | ||||
| chr2:74958876-74959038 | Rare:60 | ||||
| chr2:75199518-75199638 | Rare:22 |