| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002237-176002414 | Common:3; Rare:76 | ||||
| chr2:177212416-177212821 | Common:4; Rare:164 | ||||
| chr2:177263402-177263700 | Common:1; Rare:72 | ||||
| chr2:177264626-177264930 | Common:2; Rare:91 | ||||
| chr2:177392655-177393029 | Common:3; Rare:135; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552768-177553062 | Common:4; Rare:86 | ||||
| chr2:177618706-177619018 | Common:7; Rare:85 | ||||
| chr2:178450731-178450948 | Rare:85 | ||||
| chr2:178451090-178451378 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478411-178478659 | Common:1; Rare:79 | ||||
| chr2:180980274-180980545 | Common:1; Rare:86 | ||||
| chr2:181891665-181892137 | Common:4; Rare:189 | ||||
| chr2:183078661-183078765 | Rare:16 | ||||
| chr2:183124252-183124459 | Common:4; Rare:71 | ||||
| chr2:186486024-186486364 | Common:3; Rare:99 |