| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14947159-14947563 | Common:5; Rare:168 | ||||
| chr3:14948019-14948254 | Rare:100 | ||||
| chr3:14948357-14948675 | Common:2; Rare:98 | ||||
| chr3:15032557-15032794 | Rare:45 | ||||
| chr3:15065055-15065193 | Rare:46 | ||||
| chr3:15065199-15065342 | Common:2; Rare:62 | ||||
| chr3:15206015-15206314 | Common:1; Rare:112 | ||||
| chr3:15332368-15332690 | Common:3; Rare:98 | ||||
| chr3:15341377-15341579 | Rare:35 | ||||
| chr3:15427471-15427679 | Common:1; Rare:74 | ||||
| chr3:15601479-15601809 | Common:4; Rare:139; Clinvar:2 | ||||
| chr3:15601812-15602046 | Common:2; Rare:118; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:15859782-15860114 | Common:4; Rare:104 | ||||
| chr3:16175217-16175464 | Common:2; Rare:67 | ||||
| chr3:16264872-16265233 | Common:2; Rare:118 |