| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138608820-138609190 | Common:3; Rare:145 | ||||
| chr3:138609130-138609780 | Common:7; Rare:241 | ||||
| chr3:138834290-138835186 | Common:5; Rare:1190 | ||||
| chr3:138835295-138835695 | Common:4; Rare:93 | ||||
| chr3:138946127-138947362 | Common:10; Rare:678; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
| chr3:138947370-138947898 | Common:5; Rare:243 | ||||
| chr3:139343790-139344102 | Rare:244; Clinvar:3; Clinvar (benign):6 | ||||
| chr3:139344120-139344702 | Common:5; Rare:431; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:139344778-139345178 | Rare:107 | ||||
| chr3:139358679-139359376 | Common:4; Rare:231 | ||||
| chr3:139388793-139389333 | Common:2; Rare:138 | ||||
| chr3:139389460-139390000 | Common:17; Rare:863 | ||||
| chr3:139390066-139390184 | Rare:48 | ||||
| chr3:139677000-139677360 | Common:2; Rare:63 | ||||
| chr3:139677815-139678241 | Common:26; Rare:383 |