| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89352477-89352711 | Rare:71 | ||||
| chr12:89524748-89524896 | Common:1; Rare:27 | ||||
| chr12:89526000-89526056 | Rare:25 | ||||
| chr12:89708810-89709099 | Common:1; Rare:113 | ||||
| chr12:92145434-92145655 | Common:2; Rare:93 | ||||
| chr12:92145775-92146084 | Common:4; Rare:103 | ||||
| chr12:92146095-92146237 | Rare:46 | ||||
| chr12:93377751-93377929 | Rare:44 | ||||
| chr12:93441880-93442141 | Common:2; Rare:85 | ||||
| chr12:94459811-94460043 | Common:3; Rare:64 | ||||
| chr12:95217336-95217835 | Common:6; Rare:133 | ||||
| chr12:95474014-95474191 | Common:2; Rare:84 | ||||
| chr12:95858822-95859075 | Common:3; Rare:74 | ||||
| chr12:95996279-95996465 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:98644970-98645296 | Common:2; Rare:96 |