| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:69738572-69738989 | Common:4; Rare:147 | ||||
| chr12:71663800-71664042 | Common:1; Rare:74 | ||||
| chr12:71686026-71686113 | Common:1; Rare:23 | ||||
| chr12:71839573-71839776 | Common:2; Rare:65 | ||||
| chr12:74537701-74537873 | Common:1; Rare:66 | ||||
| chr12:75390886-75391119 | Common:1; Rare:73 | ||||
| chr12:75511569-75511706 | Rare:52 | ||||
| chr12:76084569-76084839 | Common:1; Rare:86 | ||||
| chr12:76348324-76348508 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559815-76559887 | Rare:33 | ||||
| chr12:76764051-76764276 | Common:1; Rare:93 | ||||
| chr12:76879005-76879196 | Rare:60 | ||||
| chr12:77965921-77966229 | Common:1; Rare:64 | ||||
| chr12:79934901-79935350 | Common:1; Rare:175 | ||||
| chr12:79935351-79935406 | Rare:13 |