| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9987389-9988217 | Common:6; Rare:240 | ||||
| chr3:10011010-10011580 | Common:4; Rare:251 | ||||
| chr3:10026221-10026692 | Common:2; Rare:258 | ||||
| chr3:10115447-10115762 | Common:12; Rare:294 | ||||
| chr3:10141650-10142097 | Common:5; Rare:535; Clinvar:136; Clinvar (benign):114; Clinvar (pathogenic):4 | ||||
| chr3:10248183-10248625 | Common:15; Rare:373 | ||||
| chr3:10305609-10306086 | Common:3; Rare:150 | ||||
| chr3:10321026-10321309 | Common:4; Rare:203 | ||||
| chr3:11225751-11226151 | Common:1; Rare:98 | ||||
| chr3:11272158-11272488 | Common:8; Rare:150 | ||||
| chr3:11643820-11644100 | Common:5; Rare:115 | ||||
| chr3:11718731-11719317 | Common:6; Rare:172 | ||||
| chr3:11719406-11719924 | Common:2; Rare:284 | ||||
| chr3:11720393-11720869 | Common:3; Rare:252 | ||||
| chr3:11771010-11771590 | Common:4; Rare:219 |