| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:70366688-70366873 | Common:1; Rare:43 | ||||
| chr12:71663807-71664068 | Common:1; Rare:75 | ||||
| chr12:71664253-71664491 | Rare:74 | ||||
| chr12:71686018-71686129 | Common:1; Rare:33 | ||||
| chr12:71686279-71686548 | Common:2; Rare:74 | ||||
| chr12:71754717-71754873 | Common:3; Rare:40 | ||||
| chr12:74537701-74537929 | Common:1; Rare:80 | ||||
| chr12:75390886-75391109 | Common:1; Rare:69 | ||||
| chr12:76053089-76053360 | Common:1; Rare:72 | ||||
| chr12:76083832-76084049 | Rare:60 | ||||
| chr12:76084568-76085012 | Common:4; Rare:125 | ||||
| chr12:76085015-76085079 | Common:2; Rare:13 | ||||
| chr12:76348351-76348587 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559657-76559884 | Rare:82 | ||||
| chr12:76764040-76764276 | Common:2; Rare:97 |