| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70554218-70554244 | Rare:10 | ||||
| chr2:70900241-70900636 | Common:6; Rare:106 | ||||
| chr2:70994750-70995083 | Common:4; Rare:101 | ||||
| chr2:71068139-71068353 | Rare:60 | ||||
| chr2:71068461-71068719 | Rare:127 | ||||
| chr2:71068804-71068827 | Rare:2 | ||||
| chr2:71068864-71068982 | Rare:22 | ||||
| chr2:71129723-71129742 | Rare:3 | ||||
| chr2:71129753-71130016 | Rare:52 | ||||
| chr2:71130128-71130448 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130495-71130716 | Common:4; Rare:68 | ||||
| chr2:71130730-71130811 | Rare:36 | ||||
| chr2:71227059-71227429 | Common:2; Rare:89 | ||||
| chr2:71276361-71276700 | Rare:131 | ||||
| chr2:71276791-71277083 | Common:1; Rare:63 |