| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15601512-15601804 | Common:4; Rare:123; Clinvar:1 | ||||
| chr3:16264875-16265243 | Common:2; Rare:121 | ||||
| chr3:17742596-17742938 | Common:4; Rare:116 | ||||
| chr3:19946972-19947393 | Common:5; Rare:156 | ||||
| chr3:23916916-23917188 | Rare:102 | ||||
| chr3:23917666-23917948 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr3:25789898-25790118 | Common:4; Rare:78 | ||||
| chr3:28348779-28349182 | Common:3; Rare:128 | ||||
| chr3:29280837-29281081 | Common:3; Rare:49 | ||||
| chr3:32570759-32570900 | Rare:66 | ||||
| chr3:33277325-33277415 | Common:1; Rare:19 | ||||
| chr3:33798383-33798690 | Common:2; Rare:97 | ||||
| chr3:36993094-36993549 | Common:2; Rare:146; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr3:38029613-38029873 | Common:1; Rare:52 | ||||
| chr3:39051942-39052028 | Common:1; Rare:32 |