| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:190120350-190120720 | Common:2; Rare:164; Clinvar (pathogenic):1 | ||||
| chr3:190120885-190121017 | Rare:44 | ||||
| chr3:190322409-190322538 | Common:2; Rare:33 | ||||
| chr3:193593106-193593303 | Rare:58; Clinvar:1 | ||||
| chr3:194672150-194672265 | Rare:58 | ||||
| chr3:195543215-195543449 | Common:3; Rare:89 | ||||
| chr3:196227906-196228099 | Common:2; Rare:39 | ||||
| chr3:196318163-196318336 | Common:1; Rare:77 | ||||
| chr3:196503684-196503906 | Common:3; Rare:75 | ||||
| chr3:196568518-196568768 | Common:5; Rare:77 | ||||
| chr3:196639604-196639817 | Common:2; Rare:48 | ||||
| chr3:196712193-196712358 | Common:3; Rare:55 | ||||
| chr3:196712578-196712684 | Rare:37 | ||||
| chr3:196739679-196739999 | Rare:107 | ||||
| chr3:196740020-196740119 | Common:1; Rare:33 |