| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002221-176002441 | Common:4; Rare:90 | ||||
| chr2:176129581-176129753 | Rare:93 | ||||
| chr2:176136704-176136768 | Rare:18 | ||||
| chr2:176188524-176188678 | Common:1; Rare:56 | ||||
| chr2:176269379-176269520 | Common:1; Rare:55 | ||||
| chr2:177212422-177212821 | Common:4; Rare:160 | ||||
| chr2:177263402-177263709 | Common:1; Rare:76 | ||||
| chr2:177263821-177264151 | Common:2; Rare:88 | ||||
| chr2:177264540-177264845 | Common:2; Rare:88 | ||||
| chr2:177392651-177393070 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177553058 | Common:4; Rare:91 | ||||
| chr2:177618686-177619023 | Common:7; Rare:101 | ||||
| chr2:178072745-178072836 | Rare:23 | ||||
| chr2:178450713-178450902 | Common:1; Rare:69 | ||||
| chr2:178451090-178451369 | Common:6; Rare:83; Clinvar:4; Clinvar (benign):3 |