| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127590451-127591298 | Common:15; Rare:404 | ||||
| chr3:127598137-127598539 | Common:10; Rare:309 | ||||
| chr3:127604312-127605220 | Common:6; Rare:612; Clinvar (benign):6 | ||||
| chr3:127628936-127629258 | Common:2; Rare:205 | ||||
| chr3:127672747-127673035 | Common:14; Rare:375 | ||||
| chr3:127791171-127791394 | Common:1; Rare:41 | ||||
| chr3:127791437-127791718 | Common:1; Rare:49 | ||||
| chr3:127821151-127821839 | Common:3; Rare:277 | ||||
| chr3:127822315-127822674 | Common:2; Rare:175 | ||||
| chr3:127822770-127823090 | Common:1; Rare:182 | ||||
| chr3:127823102-127823428 | Common:10; Rare:173 | ||||
| chr3:128051409-128051809 | Common:1; Rare:87 | ||||
| chr3:128052054-128052558 | Common:12; Rare:454 | ||||
| chr3:128123699-128124103 | Rare:289 | ||||
| chr3:128153318-128153643 | Common:4; Rare:201 |