| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002221-176002362 | Common:2; Rare:63 | ||||
| chr2:177212428-177212802 | Common:4; Rare:152 | ||||
| chr2:177263419-177263793 | Common:2; Rare:92 | ||||
| chr2:177264605-177264830 | Common:2; Rare:69 | ||||
| chr2:177392665-177393070 | Common:2; Rare:142; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552768-177552826 | Rare:21 | ||||
| chr2:178451090-178451354 | Common:6; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478504-178478719 | Common:1; Rare:70 | ||||
| chr2:179264508-179264861 | Common:4; Rare:132 | ||||
| chr2:182715935-182716345 | Common:3; Rare:141 | ||||
| chr2:186486037-186486344 | Common:3; Rare:86 | ||||
| chr2:189441354-189441517 | Common:2; Rare:69 | ||||
| chr2:189783977-189784125 | Common:2; Rare:56; Clinvar (benign):1 | ||||
| chr2:189784276-189784543 | Common:4; Rare:97; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190534692-190534949 | Common:2; Rare:86 |