| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15427471-15427623 | Common:1; Rare:57 | ||||
| chr3:15601510-15601804 | Common:4; Rare:124; Clinvar:1 | ||||
| chr3:15859780-15860094 | Common:4; Rare:97 | ||||
| chr3:16174483-16174821 | Common:1; Rare:79 | ||||
| chr3:16175261-16175448 | Common:2; Rare:44 | ||||
| chr3:16264864-16265243 | Common:2; Rare:129 | ||||
| chr3:17742513-17742805 | Common:3; Rare:102 | ||||
| chr3:19946974-19947514 | Common:8; Rare:198 | ||||
| chr3:20186138-20186415 | Common:4; Rare:90 | ||||
| chr3:23807188-23807279 | Rare:29 | ||||
| chr3:23916880-23917214 | Rare:128 | ||||
| chr3:23917641-23918031 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr3:24494738-24494889 | Rare:40 | ||||
| chr3:25428106-25428391 | Rare:64 | ||||
| chr3:25783363-25783634 | Common:2; Rare:95; Clinvar (benign):3 |