| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32391742-32391967 | Common:3; Rare:61 | ||||
| chr3:32502741-32502910 | Rare:54 | ||||
| chr3:32570712-32571016 | Common:1; Rare:133 | ||||
| chr3:32685051-32685398 | Rare:104 | ||||
| chr3:33097104-33097285 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33218786-33218953 | Common:3; Rare:46 | ||||
| chr3:33277312-33277489 | Common:1; Rare:46 | ||||
| chr3:33440946-33441099 | Rare:30 | ||||
| chr3:33645463-33645512 | Rare:6 | ||||
| chr3:33658997-33659145 | Common:3; Rare:32 | ||||
| chr3:33659570-33659773 | Common:1; Rare:53 | ||||
| chr3:33798503-33798670 | Common:2; Rare:60 | ||||
| chr3:33798985-33799190 | Rare:65 | ||||
| chr3:36993056-36993563 | Common:2; Rare:173; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:36993690-36993832 | Rare:59; Clinvar:1 |