| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:56801943-56802032 | Rare:29 | ||||
| chr3:57227591-57227899 | Common:3; Rare:108 | ||||
| chr3:57555975-57556339 | Rare:93 | ||||
| chr3:57597277-57597780 | Common:4; Rare:151 | ||||
| chr3:58332800-58332963 | Common:3; Rare:46 | ||||
| chr3:58577328-58577547 | Common:1; Rare:37 | ||||
| chr3:62318888-62319055 | Rare:71 | ||||
| chr3:63863786-63864157 | Common:8; Rare:125 | ||||
| chr3:63864446-63864563 | Common:2; Rare:42 | ||||
| chr3:66997982-66998351 | Common:2; Rare:95 | ||||
| chr3:67654582-67654754 | Common:2; Rare:64 | ||||
| chr3:69013214-69013424 | Rare:58 | ||||
| chr3:69013588-69013756 | Rare:45 | ||||
| chr3:72996674-72997038 | Common:2; Rare:142 | ||||
| chr3:81761504-81761735 | Common:8; Rare:84; Clinvar:1; Clinvar (benign):1 |