| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792676-9793119 | Common:3; Rare:155 | ||||
| chr3:9843963-9844169 | Common:2; Rare:81 | ||||
| chr3:9902759-9902943 | Rare:55 | ||||
| chr3:9916896-9917231 | Common:4; Rare:68 | ||||
| chr3:9933534-9933863 | Common:2; Rare:135; Clinvar:3 | ||||
| chr3:9987128-9987187 | Rare:10 | ||||
| chr3:9987343-9987564 | Common:1; Rare:59 | ||||
| chr3:10011087-10011457 | Common:2; Rare:103 | ||||
| chr3:10026287-10026496 | Rare:65 | ||||
| chr3:11154352-11154542 | Common:3; Rare:50 | ||||
| chr3:11225878-11226026 | Rare:19 | ||||
| chr3:11719422-11719605 | Rare:62 | ||||
| chr3:12288927-12289067 | Rare:30 | ||||
| chr3:12484328-12484554 | Common:5; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12545462-12545824 | Common:3; Rare:82 |