| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93571728-93571912 | Common:7; Rare:70 | ||||
| chr12:94459802-94460079 | Common:3; Rare:81 | ||||
| chr12:95003661-95003830 | Common:3; Rare:65; Clinvar (benign):3 | ||||
| chr12:95073488-95073653 | Common:1; Rare:63 | ||||
| chr12:95217377-95217774 | Common:4; Rare:111 | ||||
| chr12:95218113-95218261 | Common:2; Rare:41 | ||||
| chr12:95473997-95474294 | Common:2; Rare:128 | ||||
| chr12:95548796-95548925 | Common:3; Rare:47 | ||||
| chr12:95858811-95859075 | Common:3; Rare:79 | ||||
| chr12:95995917-95996098 | Common:2; Rare:25; Clinvar:1 | ||||
| chr12:96194247-96194577 | Common:5; Rare:108 | ||||
| chr12:96400520-96400687 | Common:1; Rare:77 | ||||
| chr12:96907195-96907290 | Rare:37 | ||||
| chr12:98515428-98515814 | Rare:130; Clinvar:4 | ||||
| chr12:98644997-98645317 | Common:2; Rare:97 |