| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74178800-74179065 | Common:3; Rare:83 | ||||
| chr2:74421563-74421768 | Rare:68 | ||||
| chr2:74440406-74440636 | Rare:59 | ||||
| chr2:74441838-74441964 | Common:1; Rare:35 | ||||
| chr2:74454860-74455138 | Rare:76 | ||||
| chr2:74458103-74458655 | Common:2; Rare:175 | ||||
| chr2:74482921-74483113 | Common:1; Rare:68 | ||||
| chr2:74507357-74507452 | Rare:28 | ||||
| chr2:74507650-74507775 | Rare:28 | ||||
| chr2:74529653-74530036 | Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530491-74530616 | Common:1; Rare:43; Clinvar:2 | ||||
| chr2:74553927-74554156 | Rare:49 | ||||
| chr2:74654089-74654285 | Common:1; Rare:50 | ||||
| chr2:74833854-74834166 | Rare:91 | ||||
| chr2:74835131-74835325 | Rare:49 |