| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123270203-123270337 | Common:1; Rare:51 | ||||
| chr12:123363754-123363911 | Common:1; Rare:48 | ||||
| chr12:123630218-123630489 | Rare:59; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:123659874-123660081 | Common:2; Rare:64 | ||||
| chr12:124566587-124566634 | Rare:5 | ||||
| chr12:125983370-125983448 | Common:6; Rare:23 | ||||
| chr12:126191237-126191336 | Rare:16 | ||||
| chr12:129904183-129904335 | Rare:38 | ||||
| chr12:132189647-132189912 | Common:6; Rare:100 | ||||
| chr12:132282765-132282805 | Common:1; Rare:8 | ||||
| chr12:132389822-132389885 | Rare:11 | ||||
| chr12:132437308-132437612 | Common:2; Rare:72 | ||||
| chr12:132446028-132446321 | Common:6; Rare:104 | ||||
| chr13:19601778-19601928 | Common:2; Rare:57 | ||||
| chr13:19671602-19671896 | Common:1; Rare:58 |