| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:151261720-151261975 | Common:4; Rare:63 | ||||
| chr2:151289161-151289767 | Common:2; Rare:119 | ||||
| chr2:151409814-151410211 | Common:2; Rare:139 | ||||
| chr2:151410295-151410424 | Rare:42 | ||||
| chr2:151410538-151410645 | Common:2; Rare:31 | ||||
| chr2:151828301-151828733 | Common:3; Rare:129 | ||||
| chr2:152098094-152098232 | Common:1; Rare:25 | ||||
| chr2:152098834-152099178 | Rare:127; Clinvar:6; Clinvar (benign):6 | ||||
| chr2:152099538-152099623 | Rare:11 | ||||
| chr2:152175375-152175602 | Rare:77 | ||||
| chr2:152175627-152176202 | Common:4; Rare:151 | ||||
| chr2:152334974-152335198 | Common:1; Rare:73 | ||||
| chr2:152717356-152717711 | Common:3; Rare:189 | ||||
| chr2:152718426-152718673 | Common:1; Rare:98 | ||||
| chr2:152718784-152718925 | Common:1; Rare:86; Clinvar:1 |