| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16512900-16513035 | Common:1; Rare:21 | ||||
| chr3:16513615-16513787 | Common:4; Rare:45 | ||||
| chr3:17742534-17742927 | Common:3; Rare:139 | ||||
| chr3:19946974-19947406 | Common:5; Rare:159 | ||||
| chr3:20186139-20186548 | Common:7; Rare:125 | ||||
| chr3:23805802-23806053 | Common:2; Rare:51 | ||||
| chr3:23916898-23917204 | Rare:120 | ||||
| chr3:23917648-23918003 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr3:25783383-25783621 | Common:2; Rare:79; Clinvar (benign):3 | ||||
| chr3:25789993-25790112 | Common:3; Rare:46 | ||||
| chr3:28241439-28241659 | Common:1; Rare:72 | ||||
| chr3:28349015-28349185 | Common:2; Rare:48 | ||||
| chr3:31532009-31532168 | Common:3; Rare:52 | ||||
| chr3:31532304-31532629 | Common:3; Rare:103 | ||||
| chr3:31980616-31980672 | Rare:9 |