| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197736877-197737221 | Common:3; Rare:111 | ||||
| chr3:197749346-197749537 | Common:2; Rare:49 | ||||
| chr3:197749669-197749972 | Common:1; Rare:103 | ||||
| chr3:197750133-197750258 | Rare:33 | ||||
| chr3:197791101-197791274 | Common:1; Rare:58 | ||||
| chr3:197949849-197950579 | Common:7; Rare:204; Clinvar (benign):2 | ||||
| chr3:197950937-197951312 | Rare:111; Clinvar (benign):1 | ||||
| chr3:197959989-197960245 | Common:1; Rare:90 | ||||
| chr4:124289-124590 | Common:7; Rare:83 | ||||
| chr4:305404-305679 | Common:2; Rare:94 | ||||
| chr4:337605-337877 | Common:1; Rare:80 | ||||
| chr4:499117-499351 | Common:3; Rare:100 | ||||
| chr4:663560-663829 | Common:1; Rare:106; Clinvar:1 | ||||
| chr4:664148-664280 | Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:673296-673562 | Rare:107 |