| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174486983-174487416 | Common:2; Rare:108 | ||||
| chr2:174682842-174683009 | Common:1; Rare:66 | ||||
| chr2:175167671-175167796 | Rare:44 | ||||
| chr2:175168104-175168558 | Common:2; Rare:121 | ||||
| chr2:175181637-175181776 | Common:3; Rare:59 | ||||
| chr2:176002214-176002420 | Common:4; Rare:86 | ||||
| chr2:176129622-176129750 | Rare:65 | ||||
| chr2:176188454-176188668 | Common:2; Rare:80 | ||||
| chr2:176188982-176189095 | Common:2; Rare:39 | ||||
| chr2:177212400-177212821 | Common:5; Rare:173 | ||||
| chr2:177213153-177213303 | Rare:64 | ||||
| chr2:177263389-177263673 | Common:1; Rare:67 | ||||
| chr2:177264539-177264892 | Common:2; Rare:101 | ||||
| chr2:177392627-177392863 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:177552754-177553109 | Common:5; Rare:111 |