| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15099127-15099282 | Rare:36 | ||||
| chr3:15205976-15206337 | Common:1; Rare:131 | ||||
| chr3:15427460-15427629 | Common:1; Rare:61 | ||||
| chr3:15601462-15601810 | Common:4; Rare:144; Clinvar:2 | ||||
| chr3:15601859-15602019 | Common:1; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:15859544-15859569 | Rare:10 | ||||
| chr3:15859787-15860094 | Common:4; Rare:95 | ||||
| chr3:16174157-16174489 | Common:5; Rare:55 | ||||
| chr3:16174495-16175106 | Common:1; Rare:129 | ||||
| chr3:16175109-16175631 | Common:3; Rare:161 | ||||
| chr3:16264866-16265243 | Common:2; Rare:128 | ||||
| chr3:16512880-16513023 | Common:1; Rare:26 | ||||
| chr3:16513588-16513973 | Common:4; Rare:105 | ||||
| chr3:16884828-16885157 | Common:6; Rare:80 | ||||
| chr3:17742596-17742943 | Common:4; Rare:120 |