| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31980754-31981083 | Common:2; Rare:142 | ||||
| chr3:31981182-31981869 | Common:12; Rare:358 | ||||
| chr3:32106344-32106765 | Common:11; Rare:297; Clinvar:8; Clinvar (benign):3 | ||||
| chr3:32106873-32107355 | Common:3; Rare:133 | ||||
| chr3:32238524-32238826 | Common:6; Rare:197 | ||||
| chr3:32391458-32392100 | Common:21; Rare:474 | ||||
| chr3:32502701-32502924 | Rare:67 | ||||
| chr3:32569940-32570444 | Common:4; Rare:255 | ||||
| chr3:32570730-32571070 | Common:3; Rare:333 | ||||
| chr3:32684762-32685459 | Rare:276 | ||||
| chr3:33096483-33096679 | Common:2; Rare:42 | ||||
| chr3:33097017-33097406 | Common:9; Rare:246; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr3:33113810-33114324 | Common:7; Rare:390; Clinvar:17; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr3:33114333-33114657 | Common:2; Rare:180; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr3:33277240-33277536 | Common:5; Rare:142 |