| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348780-28349203 | Common:4; Rare:134 | ||||
| chr3:29280846-29281407 | Common:15; Rare:109 | ||||
| chr3:31532381-31532648 | Common:3; Rare:73 | ||||
| chr3:31533016-31533305 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr3:31981625-31981808 | Common:1; Rare:49 | ||||
| chr3:32106383-32106682 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32391688-32391967 | Common:3; Rare:79 | ||||
| chr3:32570702-32570950 | Common:1; Rare:112 | ||||
| chr3:33097059-33097220 | Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:33218776-33218974 | Common:3; Rare:57 | ||||
| chr3:33277325-33277513 | Common:2; Rare:57 | ||||
| chr3:33798372-33798891 | Common:3; Rare:162 | ||||
| chr3:36993108-36993563 | Common:2; Rare:145; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37243166-37243429 | Common:1; Rare:62 | ||||
| chr3:37994086-37994171 | Rare:23 |