| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123533347-123533571 | Rare:65 | ||||
| chr12:123533651-123533876 | Common:1; Rare:63 | ||||
| chr12:123533888-123534270 | Common:4; Rare:104 | ||||
| chr12:123583978-123584121 | Rare:19 | ||||
| chr12:123584257-123584643 | Common:6; Rare:128 | ||||
| chr12:123601597-123601698 | Common:1; Rare:13 | ||||
| chr12:123601749-123601853 | Rare:18 | ||||
| chr12:123601955-123602211 | Common:4; Rare:84 | ||||
| chr12:123602332-123602344 | Rare:3 | ||||
| chr12:123602367-123602415 | Rare:11 | ||||
| chr12:123633580-123633940 | Common:2; Rare:166; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123670968-123671199 | Common:5; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:123712115-123712484 | Common:8; Rare:136; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:123761849-123762155 | Common:3; Rare:72 | ||||
| chr12:123971789-123971980 | Common:1; Rare:54 |