| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176123059-176123358 | Common:3; Rare:106 | ||||
| chr2:176129548-176129607 | Rare:32 | ||||
| chr2:176188500-176188668 | Common:1; Rare:65 | ||||
| chr2:176188987-176189246 | Common:2; Rare:106 | ||||
| chr2:176269386-176269514 | Common:1; Rare:52 | ||||
| chr2:177212416-177212821 | Common:4; Rare:164 | ||||
| chr2:177213164-177213266 | Rare:43 | ||||
| chr2:177263475-177263678 | Common:1; Rare:51 | ||||
| chr2:177264630-177264826 | Common:2; Rare:64 | ||||
| chr2:177392644-177393066 | Common:3; Rare:145; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:178451098-178451365 | Common:5; Rare:79; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:178478527-178478661 | Common:1; Rare:41 | ||||
| chr2:181891626-181892036 | Common:4; Rare:173 | ||||
| chr2:182715933-182716361 | Common:3; Rare:147 | ||||
| chr2:186486130-186486439 | Common:3; Rare:104 |