| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120201081-120201372 | Common:2; Rare:91 | ||||
| chr12:120265674-120265940 | Common:1; Rare:105 | ||||
| chr12:120437842-120438395 | Common:3; Rare:188; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446344-120446504 | Common:2; Rare:74 | ||||
| chr12:120469624-120469905 | Common:3; Rare:98 | ||||
| chr12:120495845-120496368 | Common:7; Rare:177 | ||||
| chr12:120529086-120529252 | Common:2; Rare:63 | ||||
| chr12:120534183-120534361 | Common:1; Rare:46 | ||||
| chr12:120581344-120581588 | Common:1; Rare:83 | ||||
| chr12:121210059-121210146 | Common:2; Rare:30 | ||||
| chr12:121352326-121352612 | Common:3; Rare:107 | ||||
| chr12:121399892-121400171 | Common:5; Rare:103 | ||||
| chr12:121536057-121536413 | Common:1; Rare:70 | ||||
| chr12:121580241-121580363 | Rare:43 | ||||
| chr12:121802906-121803091 | Rare:49 |