| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48439992-48440353 | Common:3; Rare:149 | ||||
| chr3:48446552-48446870 | Common:4; Rare:119 | ||||
| chr3:48446967-48447159 | Rare:65 | ||||
| chr3:48465716-48465936 | Common:3; Rare:36; Clinvar (benign):2 | ||||
| chr3:48466070-48466533 | Common:3; Rare:125; Clinvar:6; Clinvar (benign):3 | ||||
| chr3:48472686-48472913 | Common:1; Rare:40 | ||||
| chr3:48472924-48473432 | Common:2; Rare:109 | ||||
| chr3:48479216-48479300 | Rare:35 | ||||
| chr3:48503972-48504502 | Common:4; Rare:146 | ||||
| chr3:48556781-48557400 | Common:3; Rare:155 | ||||
| chr3:48609547-48609829 | Rare:99 | ||||
| chr3:48634844-48635031 | Common:1; Rare:47 | ||||
| chr3:48635336-48635763 | Common:2; Rare:122 | ||||
| chr3:48635829-48635927 | Rare:19 | ||||
| chr3:48685639-48686037 | Common:2; Rare:123 |