| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89352344-89352770 | Common:1; Rare:117 | ||||
| chr12:89524313-89524545 | Rare:84 | ||||
| chr12:89524735-89524923 | Common:2; Rare:44 | ||||
| chr12:89525870-89526109 | Common:1; Rare:90 | ||||
| chr12:89708698-89708981 | Rare:106 | ||||
| chr12:89709284-89709474 | Common:2; Rare:90 | ||||
| chr12:91180442-91180926 | Common:2; Rare:78 | ||||
| chr12:91182612-91182921 | Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:91182932-91183145 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr12:92145834-92146204 | Common:2; Rare:111 | ||||
| chr12:92929054-92929504 | Common:3; Rare:135 | ||||
| chr12:93377716-93377909 | Rare:49 | ||||
| chr12:93441879-93442142 | Common:2; Rare:86 | ||||
| chr12:93571592-93571902 | Common:7; Rare:116 | ||||
| chr12:94402516-94402599 | Common:1; Rare:11 |