| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74421582-74421771 | Rare:65 | ||||
| chr2:74465363-74465436 | Rare:18 | ||||
| chr2:74482928-74483129 | Common:1; Rare:78 | ||||
| chr2:74507289-74507375 | Rare:24 | ||||
| chr2:74507377-74507523 | Rare:39 | ||||
| chr2:74507669-74507873 | Common:1; Rare:57 | ||||
| chr2:74529642-74529964 | Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74553941-74554142 | Rare:43 | ||||
| chr2:74555624-74555791 | Common:1; Rare:49 | ||||
| chr2:74654103-74654367 | Common:1; Rare:90 | ||||
| chr2:74833854-74834153 | Rare:87 | ||||
| chr2:74958560-74958677 | Common:2; Rare:42 | ||||
| chr2:74958872-74959027 | Rare:60 | ||||
| chr2:75710630-75710779 | Common:2; Rare:58 | ||||
| chr2:80304419-80304702 | Common:3; Rare:66 |