| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:152717150-152717256 | Rare:43 | ||||
| chr2:152717356-152718086 | Common:4; Rare:326 | ||||
| chr2:152718223-152718886 | Common:3; Rare:293; Clinvar:1 | ||||
| chr2:156330405-156330522 | Common:1; Rare:24 | ||||
| chr2:156332311-156332904 | Common:2; Rare:153; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:156436015-156436525 | Common:3; Rare:138 | ||||
| chr2:157257549-157257968 | Rare:69 | ||||
| chr2:157258008-157258126 | Rare:35 | ||||
| chr2:157301844-157301941 | Rare:19 | ||||
| chr2:159136013-159136299 | Common:15; Rare:110 | ||||
| chr2:159615274-159615343 | Common:2; Rare:22 | ||||
| chr2:159615423-159615692 | Common:2; Rare:86 | ||||
| chr2:159616279-159616469 | Common:1; Rare:41 | ||||
| chr2:159712411-159712627 | Common:2; Rare:82 | ||||
| chr2:160277294-160277442 | Rare:45 |