| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50337162-50337899 | Common:3; Rare:235 | ||||
| chr3:50338063-50338241 | Common:1; Rare:33 | ||||
| chr3:50340174-50340369 | Rare:37 | ||||
| chr3:50340474-50340645 | Common:1; Rare:44 | ||||
| chr3:50340725-50340980 | Common:2; Rare:76 | ||||
| chr3:50341158-50341322 | Common:2; Rare:30 | ||||
| chr3:50350656-50350974 | Common:2; Rare:60 | ||||
| chr3:50351067-50351363 | Common:2; Rare:53 | ||||
| chr3:50359416-50359782 | Common:2; Rare:105 | ||||
| chr3:50365178-50365394 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:50503630-50503817 | Common:1; Rare:63 | ||||
| chr3:50567608-50567958 | Common:1; Rare:102 | ||||
| chr3:50569000-50569229 | Rare:45 | ||||
| chr3:50569379-50569522 | Rare:31 | ||||
| chr3:50611668-50612157 | Common:2; Rare:120; Clinvar:1 |