| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10141663-10141998 | Common:2; Rare:284; Clinvar:70; Clinvar (benign):57 | ||||
| chr3:10248251-10248656 | Common:10; Rare:252 | ||||
| chr3:10816057-10816341 | Rare:106 | ||||
| chr3:11272327-11272437 | Common:1; Rare:23 | ||||
| chr3:11719428-11719754 | Rare:98 | ||||
| chr3:12287750-12287937 | Common:5; Rare:33 | ||||
| chr3:12288760-12289180 | Common:4; Rare:145 | ||||
| chr3:12484325-12484568 | Common:10; Rare:149; Clinvar:6; Clinvar (benign):4 | ||||
| chr3:12556973-12557169 | Common:4; Rare:76 | ||||
| chr3:12663810-12664000 | Rare:65; Clinvar:6; Clinvar (benign):7 | ||||
| chr3:12664052-12664330 | Common:3; Rare:142; Clinvar:2; Clinvar (benign):7 | ||||
| chr3:12967557-12967994 | Common:8; Rare:284 | ||||
| chr3:13420168-13420462 | Common:2; Rare:151 | ||||
| chr3:13420530-13420830 | Common:4; Rare:64 | ||||
| chr3:13479989-13480389 | Common:5; Rare:190 |