| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121858685-121859162 | Common:5; Rare:105; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:122526849-122527291 | Common:4; Rare:162 | ||||
| chr12:122896055-122896240 | Rare:95 | ||||
| chr12:122975129-122975260 | Common:1; Rare:39 | ||||
| chr12:122980218-122980262 | Rare:15 | ||||
| chr12:122980571-122980969 | Common:2; Rare:114 | ||||
| chr12:123233087-123233538 | Common:2; Rare:152; Clinvar:1 | ||||
| chr12:123364785-123364989 | Common:5; Rare:83 | ||||
| chr12:123383804-123384206 | Rare:92 | ||||
| chr12:123458075-123458213 | Common:1; Rare:33 | ||||
| chr12:123584284-123584813 | Common:9; Rare:176 | ||||
| chr12:123601819-123602174 | Common:6; Rare:99 | ||||
| chr12:123633607-123633856 | Common:1; Rare:120; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972557-123972899 | Common:6; Rare:117 | ||||
| chr12:124786457-124786786 | Common:3; Rare:88 |