| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32570752-32570962 | Common:1; Rare:164 | ||||
| chr3:32703581-32703701 | Common:2; Rare:23 | ||||
| chr3:32816978-32817646 | Common:1; Rare:192 | ||||
| chr3:32817921-32818129 | Common:2; Rare:141 | ||||
| chr3:33097067-33097700 | Common:8; Rare:236; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:33113955-33114071 | Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:33277302-33277489 | Common:2; Rare:47 | ||||
| chr3:33439994-33440292 | Rare:90 | ||||
| chr3:33440520-33440890 | Common:4; Rare:103 | ||||
| chr3:33440910-33441120 | Rare:86 | ||||
| chr3:33718042-33718309 | Rare:164 | ||||
| chr3:33798435-33798704 | Common:4; Rare:151 | ||||
| chr3:33798900-33799260 | Common:1; Rare:190 | ||||
| chr3:36380306-36380933 | Common:9; Rare:263 | ||||
| chr3:36993056-36993595 | Common:4; Rare:371; Clinvar:71; Clinvar (benign):32; Clinvar (pathogenic):7 |