| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:177197438-177197690 | Common:1; Rare:63 | ||||
| chr3:179071755-179071877 | Rare:26 | ||||
| chr3:179148105-179148363 | Common:6; Rare:75 | ||||
| chr3:179451143-179451496 | Common:3; Rare:91 | ||||
| chr3:179562659-179563083 | Rare:135 | ||||
| chr3:179604610-179604905 | Common:2; Rare:121 | ||||
| chr3:180602053-180602238 | Common:1; Rare:63 | ||||
| chr3:180968411-180968525 | Rare:19 | ||||
| chr3:180989668-180989843 | Rare:67; Clinvar:1 | ||||
| chr3:183884819-183884919 | Rare:48 | ||||
| chr3:184135231-184135395 | Common:2; Rare:47; Clinvar:4 | ||||
| chr3:184155061-184155446 | Rare:92 | ||||
| chr3:184180648-184180922 | Rare:76 | ||||
| chr3:184248905-184249271 | Common:3; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:184249489-184249764 | Common:1; Rare:83 |