| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42876560-42876593 | Rare:8 | ||||
| chr3:43621894-43622312 | Common:2; Rare:120; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690633-43691013 | Common:7; Rare:165; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:44338057-44338169 | Common:2; Rare:38 | ||||
| chr3:44338331-44338518 | Common:3; Rare:67 | ||||
| chr3:44338715-44338813 | Common:2; Rare:33 | ||||
| chr3:44477609-44477758 | Common:1; Rare:37 | ||||
| chr3:44510574-44510789 | Common:4; Rare:60 | ||||
| chr3:44624941-44625095 | Common:2; Rare:44 | ||||
| chr3:44729552-44729667 | Common:1; Rare:44 | ||||
| chr3:44761583-44761844 | Common:3; Rare:97 | ||||
| chr3:44861767-44861927 | Common:2; Rare:72 | ||||
| chr3:44976091-44976278 | Common:2; Rare:76 | ||||
| chr3:45689207-45689468 | Common:1; Rare:92 | ||||
| chr3:45995776-45995850 | Rare:18; Clinvar:1 |