| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139083686-139083855 | Rare:35 | ||||
| chr4:139083873-139083953 | Common:1; Rare:23 | ||||
| chr4:139084150-139084617 | Common:4; Rare:188 | ||||
| chr4:139177212-139177491 | Rare:79 | ||||
| chr4:139295140-139295418 | Common:3; Rare:66 | ||||
| chr4:139295507-139295578 | Rare:13 | ||||
| chr4:139295727-139295898 | Common:1; Rare:60 | ||||
| chr4:139301181-139301577 | Common:6; Rare:112 | ||||
| chr4:139301890-139302080 | Common:2; Rare:45 | ||||
| chr4:139302150-139302616 | Common:4; Rare:104 | ||||
| chr4:139452866-139453205 | Common:3; Rare:64 | ||||
| chr4:139453361-139453465 | Rare:19 | ||||
| chr4:139453532-139453867 | Common:2; Rare:107; Clinvar:4 | ||||
| chr4:139453942-139454241 | Common:3; Rare:95; Clinvar:5; Clinvar (benign):4 | ||||
| chr4:139665691-139666031 | Common:2; Rare:78 |