| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98531430-98531734 | Common:2; Rare:71 | ||||
| chr12:98634109-98634205 | Rare:12 | ||||
| chr12:98634359-98634529 | Rare:33 | ||||
| chr12:100281059-100281298 | Common:1; Rare:35 | ||||
| chr12:100564238-100564543 | Rare:58 | ||||
| chr12:100572854-100573132 | Common:3; Rare:53 | ||||
| chr12:101379221-101379413 | Rare:39 | ||||
| chr12:101381045-101381209 | Rare:37 | ||||
| chr12:101719887-101720255 | Common:6; Rare:74 | ||||
| chr12:101723562-101723848 | Common:2; Rare:70 | ||||
| chr12:101780562-101780755 | Common:1; Rare:49; Clinvar (pathogenic):1 | ||||
| chr12:101901905-101901923 | Rare:2 | ||||
| chr12:102025713-102026010 | Rare:50 | ||||
| chr12:102126594-102126760 | Common:1; Rare:36 | ||||
| chr12:103440445-103440450 |