| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124703-14125021 | Common:3; Rare:85; Clinvar:2 | ||||
| chr3:14178573-14178870 | Common:2; Rare:153; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:15427510-15427618 | Rare:36 | ||||
| chr3:15601519-15601746 | Common:4; Rare:91 | ||||
| chr3:16264907-16265220 | Common:2; Rare:94 | ||||
| chr3:19947060-19947399 | Common:4; Rare:129 | ||||
| chr3:20186176-20186485 | Common:3; Rare:101 | ||||
| chr3:23916898-23917177 | Rare:107 | ||||
| chr3:32106418-32106636 | Common:4; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33798520-33798635 | Common:2; Rare:32 | ||||
| chr3:40457204-40457368 | Common:2; Rare:79 | ||||
| chr3:40524819-40525011 | Common:1; Rare:55 | ||||
| chr3:42160048-42160264 | Common:2; Rare:42 | ||||
| chr3:42804451-42804649 | Common:2; Rare:56 | ||||
| chr3:44761590-44761794 | Common:3; Rare:73 |