| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171433991-171434246 | Common:1; Rare:65 | ||||
| chr2:171894211-171894313 | Rare:53; Clinvar:1 | ||||
| chr2:171922288-171922503 | Rare:82 | ||||
| chr2:171999822-171999972 | Common:1; Rare:63 | ||||
| chr2:174248465-174248731 | Common:1; Rare:79 | ||||
| chr2:174395624-174395795 | Common:2; Rare:56 | ||||
| chr2:175181654-175181830 | Common:3; Rare:62 | ||||
| chr2:176002257-176002351 | Common:1; Rare:41 | ||||
| chr2:177212435-177212802 | Common:4; Rare:148 | ||||
| chr2:177263410-177263595 | Rare:41 | ||||
| chr2:177263812-177263884 | Rare:18 | ||||
| chr2:177264618-177264887 | Common:2; Rare:83 | ||||
| chr2:177392655-177393059 | Common:3; Rare:141; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552770-177553068 | Common:4; Rare:86 | ||||
| chr2:178451077-178451378 | Common:6; Rare:87; Clinvar:4; Clinvar (benign):3 |