| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120201096-120201354 | Common:2; Rare:80 | ||||
| chr12:120446364-120446474 | Common:1; Rare:50 | ||||
| chr12:120469568-120469873 | Common:2; Rare:109 | ||||
| chr12:120495875-120496228 | Common:6; Rare:116 | ||||
| chr12:122526927-122527281 | Common:3; Rare:109 | ||||
| chr12:122980571-122980725 | Rare:49 | ||||
| chr12:123233113-123233486 | Common:2; Rare:116; Clinvar:1 | ||||
| chr12:123584336-123584609 | Common:5; Rare:91 | ||||
| chr12:123602023-123602131 | Common:3; Rare:35 | ||||
| chr12:123633624-123633845 | Common:1; Rare:101; Clinvar:8; Clinvar (benign):1 | ||||
| chr13:21176484-21176704 | Common:2; Rare:97 | ||||
| chr13:23889350-23889567 | Common:1; Rare:74 | ||||
| chr13:24922830-24923115 | Common:2; Rare:98; Clinvar:1 | ||||
| chr13:25301502-25301706 | Common:1; Rare:79 | ||||
| chr13:30465828-30466119 | Common:1; Rare:88 |