| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15601452-15601818 | Common:5; Rare:152; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:15601859-15602026 | Common:1; Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:15859526-15860236 | Common:9; Rare:217 | ||||
| chr3:16264787-16265267 | Common:4; Rare:167 | ||||
| chr3:16513623-16513734 | Common:3; Rare:32 | ||||
| chr3:16884886-16885379 | Common:8; Rare:125 | ||||
| chr3:18444667-18444973 | Common:1; Rare:64 | ||||
| chr3:18445003-18445278 | Rare:80 | ||||
| chr3:19934162-19934254 | Rare:23 | ||||
| chr3:19946894-19947567 | Common:12; Rare:242 | ||||
| chr3:20186084-20186415 | Common:4; Rare:105 | ||||
| chr3:21751071-21751364 | Common:2; Rare:91 | ||||
| chr3:23202925-23203265 | Common:1; Rare:119 | ||||
| chr3:23805713-23805775 | Common:1; Rare:16 | ||||
| chr3:23805790-23806076 | Common:2; Rare:55 |