Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:144332455-144332720 | Rare:101 | ||||
chr2:148020642-148021121 | Common:2; Rare:111; Clinvar (benign):2 | ||||
chr2:148021502-148021679 | Rare:38; Clinvar (benign):1 | ||||
chr2:151289602-151289663 | Rare:20 | ||||
chr2:151828336-151828620 | Common:3; Rare:87 | ||||
chr2:152717831-152718092 | Rare:101 | ||||
chr2:152718495-152718685 | Rare:82 | ||||
chr2:156332678-156332904 | Rare:69; Clinvar:2 | ||||
chr2:156435495-156435552 | Rare:12 | ||||
chr2:156436015-156436224 | Rare:49 | ||||
chr2:159286638-159286913 | Common:5; Rare:106 | ||||
chr2:159516537-159516665 | Common:1; Rare:15 | ||||
chr2:159615216-159615343 | Common:2; Rare:29 | ||||
chr2:159615556-159615778 | Common:1; Rare:66 | ||||
chr2:159616417-159616472 | Common:1; Rare:17 |