| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123328794-123329031 | Common:1; Rare:57 | ||||
| chr12:124340142-124340410 | Common:5; Rare:134 | ||||
| chr12:124358466-124358609 | Common:3; Rare:29 | ||||
| chr12:130812878-130812970 | Rare:12 | ||||
| chr12:130875639-130875905 | Common:2; Rare:52 | ||||
| chr12:131713500-131713531 | Rare:3 | ||||
| chr12:131939043-131939275 | Common:1; Rare:72; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:132129192-132129500 | Common:2; Rare:48 | ||||
| chr12:132189687-132190020 | Common:5; Rare:112 | ||||
| chr12:132570099-132570458 | Common:6; Rare:134 | ||||
| chr12:133140583-133140663 | Common:2; Rare:14 | ||||
| chr13:19676083-19676374 | Common:1; Rare:56 | ||||
| chr13:20995319-20995419 | Rare:16 | ||||
| chr13:20995421-20995437 | Rare:4 | ||||
| chr13:20996416-20996437 | Rare:1 |