| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51941875-51942125 | Common:2; Rare:68 | ||||
| chr3:51975048-51975111 | Common:1; Rare:19 | ||||
| chr3:51983437-51983535 | Rare:20 | ||||
| chr3:52239058-52239322 | Common:2; Rare:84 | ||||
| chr3:52287719-52287844 | Common:2; Rare:45 | ||||
| chr3:52455412-52455630 | Common:2; Rare:66 | ||||
| chr3:52685551-52685792 | Common:1; Rare:62 | ||||
| chr3:52685937-52686090 | Common:2; Rare:64 | ||||
| chr3:52705548-52706213 | Common:4; Rare:210 | ||||
| chr3:52770913-52771025 | Common:2; Rare:26 | ||||
| chr3:53130405-53130523 | Common:1; Rare:39; Clinvar (benign):3 | ||||
| chr3:53347525-53347734 | Common:1; Rare:64 | ||||
| chr3:53882106-53882368 | Common:3; Rare:88 | ||||
| chr3:56557086-56557228 | Common:2; Rare:54 | ||||
| chr3:57079292-57079424 | Common:2; Rare:38 |