| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:67269582-67269665 | Rare:25 | ||||
| chr12:68332363-68332619 | Common:1; Rare:70 | ||||
| chr12:68610733-68611041 | Common:1; Rare:125 | ||||
| chr12:68686829-68687016 | Common:4; Rare:50 | ||||
| chr12:68808834-68809047 | Rare:39 | ||||
| chr12:69359678-69359794 | Common:3; Rare:47 | ||||
| chr12:69470317-69470429 | Common:2; Rare:37 | ||||
| chr12:71663812-71664067 | Common:1; Rare:70 | ||||
| chr12:74537753-74537857 | Rare:41 | ||||
| chr12:75390876-75391105 | Common:1; Rare:67 | ||||
| chr12:75480629-75480881 | Rare:52 | ||||
| chr12:76348356-76348521 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76764051-76764261 | Common:1; Rare:87 | ||||
| chr12:76878993-76879247 | Rare:84 | ||||
| chr12:77939996-77940337 | Common:2; Rare:63 |