| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:86991084-86991426 | Common:1; Rare:87 | ||||
| chr3:87227100-87227352 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058937-88059293 | Common:2; Rare:130 | ||||
| chr3:88149490-88149760 | Common:1; Rare:58 | ||||
| chr3:88149787-88150000 | Rare:55 | ||||
| chr3:89107420-89107780 | Common:2; Rare:99 | ||||
| chr3:93973890-93974020 | Rare:32; Clinvar:1 | ||||
| chr3:93974040-93974320 | Common:1; Rare:55 | ||||
| chr3:93979907-93980252 | Common:4; Rare:134; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:93980328-93980757 | Rare:206; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:94062689-94063083 | Common:4; Rare:97 | ||||
| chr3:97764373-97764573 | Rare:69 | ||||
| chr3:97764639-97764810 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821854-97822105 | Rare:91 | ||||
| chr3:97972220-97972610 | Common:5; Rare:112 |