| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:19527281-19527450 | Common:2; Rare:40 | ||||
| chr12:21448297-21448590 | Common:2; Rare:45 | ||||
| chr12:21451827-21452138 | Common:2; Rare:63; Clinvar (pathogenic):1 | ||||
| chr12:21509787-21510017 | Common:1; Rare:36 | ||||
| chr12:22653298-22653497 | Rare:27 | ||||
| chr12:23129129-23129332 | Common:1; Rare:25 | ||||
| chr12:23984992-23985187 | Rare:31 | ||||
| chr12:25999552-25999630 | Rare:17 | ||||
| chr12:26126143-26126367 | Rare:53 | ||||
| chr12:26455079-26455337 | Common:1; Rare:40 | ||||
| chr12:26556756-26556767 | Rare:2 | ||||
| chr12:27179836-27180057 | Rare:29 | ||||
| chr12:27428836-27429089 | Common:1; Rare:32 | ||||
| chr12:27532279-27532445 | Common:1; Rare:17 | ||||
| chr12:27616544-27616562 | Rare:4 |