| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177392850-177393280 | Common:5; Rare:203; Clinvar:9; Clinvar (benign):4 | ||||
| chr2:177552761-177553099 | Common:8; Rare:187 | ||||
| chr2:177618630-177619200 | Common:14; Rare:256 | ||||
| chr2:178194306-178194653 | Common:3; Rare:179 | ||||
| chr2:178450704-178450885 | Common:2; Rare:121 | ||||
| chr2:178451090-178451454 | Common:11; Rare:209; Clinvar:7; Clinvar (benign):6 | ||||
| chr2:178478534-178478661 | Common:2; Rare:67 | ||||
| chr2:178480184-178480489 | Common:2; Rare:90 | ||||
| chr2:180007061-180007410 | Common:2; Rare:116 | ||||
| chr2:180980090-180980400 | Common:1; Rare:75 | ||||
| chr2:180980419-180980642 | Rare:145 | ||||
| chr2:181891593-181892284 | Common:12; Rare:560 | ||||
| chr2:181892446-181892601 | Common:1; Rare:46 | ||||
| chr2:182426873-182427519 | Rare:138 | ||||
| chr2:182715887-182716454 | Common:6; Rare:336 |