| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47758167-47758271 | Common:1; Rare:17 | ||||
| chr12:47758430-47758569 | Rare:31 | ||||
| chr12:47758716-47759011 | Common:1; Rare:54 | ||||
| chr12:47773114-47773259 | Rare:55 | ||||
| chr12:48105832-48105941 | Rare:27 | ||||
| chr12:48105988-48106206 | Common:2; Rare:71 | ||||
| chr12:48106277-48106375 | Rare:29 | ||||
| chr12:48119190-48119422 | Common:2; Rare:46; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48119637-48119893 | Common:1; Rare:52 | ||||
| chr12:48122470-48122865 | Common:2; Rare:67; Clinvar:2 | ||||
| chr12:48350766-48350957 | Rare:69 | ||||
| chr12:48716671-48716929 | Common:4; Rare:83 | ||||
| chr12:48814630-48814875 | Rare:41 | ||||
| chr12:48818583-48818793 | Common:1; Rare:72 | ||||
| chr12:48852127-48852403 | Common:2; Rare:71 |