| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15601469-15601819 | Common:5; Rare:146; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:15601859-15602050 | Common:1; Rare:98; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:16264872-16265243 | Common:2; Rare:124 | ||||
| chr3:16884822-16885259 | Common:8; Rare:104 | ||||
| chr3:17742569-17742952 | Common:4; Rare:142 | ||||
| chr3:19946974-19947245 | Common:4; Rare:97 | ||||
| chr3:20186176-20186377 | Common:1; Rare:56 | ||||
| chr3:23202921-23203214 | Common:1; Rare:102 | ||||
| chr3:23916858-23917208 | Rare:134 | ||||
| chr3:23917611-23918031 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr3:24494716-24494917 | Rare:55 | ||||
| chr3:24495171-24495533 | Common:6; Rare:99 | ||||
| chr3:25428107-25428346 | Rare:52 | ||||
| chr3:25789887-25790124 | Common:4; Rare:85 | ||||
| chr3:28348592-28348672 | Rare:16 |