| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177264630-177264844 | Common:2; Rare:68 | ||||
| chr2:177392641-177393044 | Common:3; Rare:141; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552750-177552826 | Rare:30 | ||||
| chr2:178451090-178451363 | Common:6; Rare:82; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:181457253-181457565 | Common:2; Rare:109 | ||||
| chr2:181458063-181458278 | Common:1; Rare:65 | ||||
| chr2:181891665-181892036 | Common:4; Rare:152 | ||||
| chr2:186486018-186486348 | Common:3; Rare:92 | ||||
| chr2:188292692-188292869 | Common:1; Rare:44 | ||||
| chr2:188974360-188974562 | Rare:58; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189441086-189441511 | Common:2; Rare:130 | ||||
| chr2:189783965-189784085 | Common:3; Rare:42; Clinvar (benign):1 | ||||
| chr2:189784275-189784512 | Common:3; Rare:78; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:190534651-190534913 | Common:1; Rare:81 | ||||
| chr2:191014124-191014353 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):2 |