| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174486994-174487410 | Common:2; Rare:103 | ||||
| chr2:175004919-175005538 | Common:3; Rare:207; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:175167671-175167861 | Rare:64 | ||||
| chr2:175167873-175167937 | Rare:12 | ||||
| chr2:175168100-175168559 | Common:2; Rare:122 | ||||
| chr2:175181644-175181776 | Common:3; Rare:54 | ||||
| chr2:176002220-176002440 | Common:4; Rare:90 | ||||
| chr2:176269377-176269527 | Common:1; Rare:59 | ||||
| chr2:177212400-177212836 | Common:5; Rare:178 | ||||
| chr2:177392620-177393059 | Common:4; Rare:147; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552764-177552856 | Common:1; Rare:29 | ||||
| chr2:177618706-177619023 | Common:7; Rare:88 | ||||
| chr2:178194381-178194653 | Common:2; Rare:75 | ||||
| chr2:178450693-178450889 | Common:1; Rare:67 | ||||
| chr2:178451053-178451303 | Common:5; Rare:77; Clinvar:4; Clinvar (benign):3 |