| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526871-122527301 | Common:4; Rare:152 | ||||
| chr12:122974564-122974817 | Rare:56 | ||||
| chr12:122975116-122975254 | Common:1; Rare:38 | ||||
| chr12:122980571-122980950 | Common:2; Rare:108 | ||||
| chr12:123233087-123233506 | Common:2; Rare:142; Clinvar:1 | ||||
| chr12:123364820-123364952 | Common:1; Rare:51 | ||||
| chr12:123584359-123584753 | Common:7; Rare:140 | ||||
| chr12:123601819-123602174 | Common:6; Rare:99 | ||||
| chr12:123633597-123633851 | Common:1; Rare:123; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972550-123972934 | Common:6; Rare:129 | ||||
| chr12:124863602-124864056 | Common:5; Rare:123 | ||||
| chr12:124914804-124915047 | Common:3; Rare:97 | ||||
| chr12:128824046-128824141 | Common:2; Rare:42 | ||||
| chr12:128853393-128853645 | Common:2; Rare:70 | ||||
| chr12:130871730-130872122 | Common:4; Rare:164 |