| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131929521-131930290 | Common:6; Rare:555; Clinvar:4; Clinvar (benign):17 | ||||
| chr12:131949592-131950107 | Common:7; Rare:464 | ||||
| chr12:132083948-132084379 | Common:14; Rare:231 | ||||
| chr12:132142724-132143665 | Common:6; Rare:742 | ||||
| chr12:132144092-132144548 | Common:7; Rare:372 | ||||
| chr12:132144645-132145303 | Common:4; Rare:400 | ||||
| chr12:132275160-132275450 | Common:7; Rare:122 | ||||
| chr12:132489778-132490281 | Common:15; Rare:386 | ||||
| chr12:132559839-132560207 | Common:1; Rare:273 | ||||
| chr12:132560397-132560797 | Common:2; Rare:130 | ||||
| chr12:132618596-132618797 | Common:3; Rare:117; Clinvar (benign):1 | ||||
| chr12:132686776-132687047 | Rare:82 | ||||
| chr12:132687138-132687719 | Common:13; Rare:535; Clinvar:42; Clinvar (benign):41; Clinvar (pathogenic):3 | ||||
| chr12:132710446-132711003 | Common:15; Rare:449 | ||||
| chr12:132710970-132711511 | Common:12; Rare:309 |