| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31729025-31729213 | Rare:56 | ||||
| chr12:31959262-31959482 | Common:2; Rare:70 | ||||
| chr12:32502003-32502227 | Common:2; Rare:46; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:38905561-38905669 | Common:3; Rare:29 | ||||
| chr12:39619783-39619919 | Common:1; Rare:25 | ||||
| chr12:42238176-42238490 | Common:2; Rare:106 | ||||
| chr12:42325971-42325978 | Rare:2 | ||||
| chr12:42326023-42326207 | Common:1; Rare:60 | ||||
| chr12:43758753-43759007 | Common:2; Rare:72; Clinvar:2 | ||||
| chr12:43806241-43806412 | Common:2; Rare:58 | ||||
| chr12:45215982-45216188 | Common:1; Rare:66 | ||||
| chr12:45990434-45990959 | Common:2; Rare:168 | ||||
| chr12:46268984-46269246 | Common:1; Rare:50 | ||||
| chr12:46372719-46372954 | Rare:103 | ||||
| chr12:46832427-46832451 | Rare:2 |