| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57195769-57196088 | Common:3; Rare:88 | ||||
| chr12:57569119-57569277 | Common:3; Rare:37; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr12:57935906-57936216 | Common:4; Rare:79 | ||||
| chr12:62603493-62603609 | Common:1; Rare:36 | ||||
| chr12:63821826-63821966 | Common:1; Rare:45 | ||||
| chr12:65881568-65881727 | Rare:37 | ||||
| chr12:74540140-74540467 | Common:3; Rare:58 | ||||
| chr12:77324783-77325086 | Common:2; Rare:99 | ||||
| chr12:78036280-78036303 | Common:1; Rare:3 | ||||
| chr12:94873653-94873840 | Common:2; Rare:51 | ||||
| chr12:97462659-97462841 | Rare:45 | ||||
| chr12:103946663-103946933 | Rare:71 | ||||
| chr12:104030540-104030773 | Common:1; Rare:31 | ||||
| chr12:108822823-108823100 | Common:2; Rare:42 | ||||
| chr12:109111035-109111201 | Common:1; Rare:48 |