| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74958872-74959038 | Rare:62 | ||||
| chr2:75199509-75199675 | Rare:28 | ||||
| chr2:75710669-75710758 | Common:1; Rare:36 | ||||
| chr2:84441074-84441333 | Common:2; Rare:75; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:84459219-84459581 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905464-84905949 | Common:2; Rare:146 | ||||
| chr2:84906577-84906746 | Common:1; Rare:29 | ||||
| chr2:85327915-85328066 | Common:1; Rare:68 | ||||
| chr2:85354419-85354790 | Common:1; Rare:125 | ||||
| chr2:85376672-85376897 | Common:1; Rare:31 | ||||
| chr2:85539072-85539375 | Common:3; Rare:145; Clinvar (benign):7 | ||||
| chr2:85561431-85561590 | Rare:60; Clinvar:4 | ||||
| chr2:85584312-85584466 | Common:1; Rare:44 | ||||
| chr2:85595555-85595778 | Common:2; Rare:73 | ||||
| chr2:85602384-85602487 | Common:1; Rare:18 |