| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171687594-171687828 | Rare:62 | ||||
| chr2:171894221-171894364 | Rare:61; Clinvar:1 | ||||
| chr2:171922285-171922567 | Rare:99 | ||||
| chr2:171999866-171999975 | Common:1; Rare:49 | ||||
| chr2:173965232-173965513 | Common:1; Rare:98 | ||||
| chr2:174395616-174395772 | Common:2; Rare:50 | ||||
| chr2:175168117-175168511 | Common:2; Rare:103 | ||||
| chr2:175181359-175181762 | Common:7; Rare:144 | ||||
| chr2:176002195-176002389 | Common:3; Rare:78 | ||||
| chr2:177212471-177212802 | Common:3; Rare:136 | ||||
| chr2:177216699-177216947 | Rare:81 | ||||
| chr2:177264648-177264865 | Common:2; Rare:71 | ||||
| chr2:177392649-177392815 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:177393026-177393084 | Rare:12 | ||||
| chr2:178451082-178451424 | Common:6; Rare:102; Clinvar:4; Clinvar (benign):3 |