| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:63864086-63864150 | Rare:18 | ||||
| chr3:64013575-64013781 | Common:2; Rare:60 | ||||
| chr3:67654566-67654809 | Common:2; Rare:93 | ||||
| chr3:69013191-69013291 | Rare:24 | ||||
| chr3:69084811-69085096 | Common:3; Rare:80 | ||||
| chr3:69739297-69739502 | Rare:66 | ||||
| chr3:71065387-71065610 | Common:1; Rare:44 | ||||
| chr3:71130522-71130716 | Common:1; Rare:73; Clinvar:2 | ||||
| chr3:73624920-73625095 | Common:4; Rare:51 | ||||
| chr3:87227201-87227356 | Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058913-88059335 | Common:3; Rare:162 | ||||
| chr3:88149862-88150012 | Rare:49 | ||||
| chr3:93979935-93980154 | Common:1; Rare:71 | ||||
| chr3:94062887-94063083 | Rare:50 | ||||
| chr3:98593206-98593502 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 |