| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123358002-123358222 | Common:1; Rare:52 | ||||
| chr11:123511163-123511504 | Rare:72 | ||||
| chr11:123653747-123653922 | Rare:49; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:133947987-133948069 | Common:2; Rare:24 | ||||
| chr11:133948180-133948364 | Rare:30 | ||||
| chr11:134032708-134032835 | Rare:27 | ||||
| chr11:135007847-135008025 | Rare:36 | ||||
| chr12:3490215-3490499 | Common:1; Rare:37 | ||||
| chr12:3492756-3492965 | Rare:36 | ||||
| chr12:4275433-4275563 | Common:2; Rare:16 | ||||
| chr12:5430217-5430433 | Rare:41 | ||||
| chr12:6226068-6226335 | Common:1; Rare:47 | ||||
| chr12:6770156-6770569 | Rare:115 | ||||
| chr12:7960872-7960934 | Common:1; Rare:14 | ||||
| chr12:7970684-7970977 | Common:1; Rare:86 |