| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10248878-10248947 | Rare:13 | ||||
| chr3:10249281-10249498 | Common:1; Rare:93 | ||||
| chr3:10292889-10293148 | Common:1; Rare:56 | ||||
| chr3:10293304-10293325 | Rare:3 | ||||
| chr3:10320996-10321307 | Common:2; Rare:123 | ||||
| chr3:11272172-11272506 | Common:4; Rare:81 | ||||
| chr3:11272637-11272725 | Rare:17 | ||||
| chr3:11581784-11581998 | Common:2; Rare:44 | ||||
| chr3:11643863-11644080 | Common:2; Rare:66 | ||||
| chr3:11719596-11719815 | Common:1; Rare:68 | ||||
| chr3:11846690-11847059 | Common:2; Rare:100 | ||||
| chr3:12287641-12287783 | Common:3; Rare:36 | ||||
| chr3:12484155-12484775 | Common:9; Rare:174; Clinvar:10; Clinvar (benign):4 | ||||
| chr3:12556822-12557250 | Common:5; Rare:135 | ||||
| chr3:12557278-12557478 | Common:4; Rare:51 |