| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120495871-120496246 | Common:7; Rare:125 | ||||
| chr12:120497773-120498144 | Rare:74 | ||||
| chr12:120529090-120529415 | Common:2; Rare:90 | ||||
| chr12:120534308-120534363 | Rare:23 | ||||
| chr12:120581344-120581505 | Rare:62 | ||||
| chr12:120686967-120687182 | Common:1; Rare:74 | ||||
| chr12:120687366-120687531 | Rare:43 | ||||
| chr12:120978499-120978859 | Common:3; Rare:117; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr12:120978883-120978955 | Rare:31; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:120979121-120979225 | Common:1; Rare:21 | ||||
| chr12:121210059-121210257 | Common:2; Rare:81 | ||||
| chr12:121296697-121296928 | Common:1; Rare:69 | ||||
| chr12:121352323-121352612 | Common:3; Rare:110 | ||||
| chr12:121399885-121400189 | Common:5; Rare:112 | ||||
| chr12:121580226-121580438 | Rare:65 |