| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50365203-50365373 | Common:1; Rare:63 | ||||
| chr3:50569386-50569569 | Common:1; Rare:41 | ||||
| chr3:50611756-50611859 | Rare:25 | ||||
| chr3:51385106-51385349 | Common:2; Rare:86 | ||||
| chr3:51499952-51500112 | Rare:36 | ||||
| chr3:51983361-51983540 | Rare:37 | ||||
| chr3:52239056-52239273 | Common:2; Rare:73 | ||||
| chr3:52287727-52287871 | Common:2; Rare:54 | ||||
| chr3:52403290-52403453 | Rare:57; Clinvar:4; Clinvar (benign):8 | ||||
| chr3:52409893-52410061 | Rare:52 | ||||
| chr3:52410354-52410679 | Rare:67 | ||||
| chr3:52455392-52455665 | Common:2; Rare:87 | ||||
| chr3:52685579-52685694 | Rare:31 | ||||
| chr3:52685776-52686095 | Common:3; Rare:117 | ||||
| chr3:52693607-52693658 | Rare:15 |