| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176188488-176188666 | Common:1; Rare:67 | ||||
| chr2:176188940-176189145 | Common:2; Rare:75 | ||||
| chr2:176269339-176269607 | Common:2; Rare:92 | ||||
| chr2:177212131-177212239 | Common:1; Rare:21 | ||||
| chr2:177212353-177212821 | Common:5; Rare:185 | ||||
| chr2:177213159-177213280 | Rare:53 | ||||
| chr2:177263427-177263725 | Common:2; Rare:73 | ||||
| chr2:177264630-177264930 | Common:2; Rare:91 | ||||
| chr2:177392597-177392905 | Common:2; Rare:102; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:177552651-177552856 | Common:1; Rare:91 | ||||
| chr2:177618686-177619023 | Common:7; Rare:101 | ||||
| chr2:178112281-178112597 | Common:2; Rare:104 | ||||
| chr2:178450693-178450874 | Common:1; Rare:61 | ||||
| chr2:178451090-178451418 | Common:6; Rare:99; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478507-178478686 | Common:1; Rare:60 |