| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46831873-46831897 | Rare:8 | ||||
| chr12:47789311-47789413 | Rare:26 | ||||
| chr12:49028880-49029086 | Common:3; Rare:57; Clinvar (benign):2 | ||||
| chr12:49029231-49029426 | Rare:47; Clinvar (benign):1 | ||||
| chr12:49052640-49052927 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:52004753-52004902 | Rare:21 | ||||
| chr12:52147323-52147671 | Common:3; Rare:94 | ||||
| chr12:52183261-52183542 | Rare:53 | ||||
| chr12:52208616-52208857 | Common:2; Rare:41 | ||||
| chr12:52514391-52514649 | Common:8; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:52522728-52522786 | Common:2; Rare:17 | ||||
| chr12:52642057-52642124 | Rare:5 | ||||
| chr12:52660063-52660195 | Rare:22 | ||||
| chr12:52675968-52676602 | Common:4; Rare:141; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:52867657-52867858 | Rare:36 |