| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179604564-179604912 | Common:3; Rare:146 | ||||
| chr3:179652595-179652778 | Common:1; Rare:32 | ||||
| chr3:179652880-179653145 | Common:1; Rare:75 | ||||
| chr3:180602106-180602270 | Common:1; Rare:60 | ||||
| chr3:180679457-180679568 | Rare:23; Clinvar:3 | ||||
| chr3:180989517-180989843 | Rare:131; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:181711674-181712497 | Common:1; Rare:212; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:182793334-182793610 | Common:3; Rare:77 | ||||
| chr3:182980083-182980276 | Common:1; Rare:51 | ||||
| chr3:182980490-182980606 | Rare:39 | ||||
| chr3:182980673-182980755 | Rare:23 | ||||
| chr3:183099442-183099690 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183254359-183254427 | Rare:16 | ||||
| chr3:183428559-183428676 | Common:1; Rare:37 | ||||
| chr3:183635487-183635705 | Common:3; Rare:70 |