| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:13044338-13044392 | Rare:14 | ||||
| chr12:14385162-14385391 | Rare:45 | ||||
| chr12:14771117-14771270 | Rare:54 | ||||
| chr12:14774178-14774460 | Common:3; Rare:74 | ||||
| chr12:14803457-14803715 | Common:1; Rare:68 | ||||
| chr12:14948852-14949003 | Common:1; Rare:24 | ||||
| chr12:14961546-14961673 | Common:2; Rare:36 | ||||
| chr12:15882261-15882580 | Common:1; Rare:102 | ||||
| chr12:15984952-15985243 | Common:1; Rare:46 | ||||
| chr12:16347476-16347724 | Common:4; Rare:49 | ||||
| chr12:16606469-16606748 | Rare:62 | ||||
| chr12:21437627-21437697 | Common:3; Rare:33 | ||||
| chr12:21501538-21501835 | Common:2; Rare:81 | ||||
| chr12:21657778-21657974 | Common:4; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22544195-22544284 | Rare:40 |