| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47795297-47795487 | Common:2; Rare:45 | ||||
| chr12:47963489-47963649 | Rare:46 | ||||
| chr12:48105985-48106132 | Common:1; Rare:41 | ||||
| chr12:48106276-48106332 | Rare:12 | ||||
| chr12:48119193-48119379 | Common:2; Rare:34; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48350771-48350907 | Rare:49 | ||||
| chr12:48815445-48815617 | Common:1; Rare:41 | ||||
| chr12:48903862-48904188 | Common:8; Rare:79 | ||||
| chr12:49018736-49018935 | Common:1; Rare:83 | ||||
| chr12:49131341-49131628 | Common:2; Rare:112 | ||||
| chr12:49188482-49188630 | Common:2; Rare:20 | ||||
| chr12:49189183-49189486 | Rare:51 | ||||
| chr12:49264775-49265092 | Common:4; Rare:113 | ||||
| chr12:49323017-49323277 | Common:1; Rare:60 | ||||
| chr12:49568104-49568211 | Common:2; Rare:36 |