Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:135876371-135876646 | Common:1; Rare:76 | ||||
chr2:135985404-135985685 | Common:4; Rare:125; Clinvar (benign):1 | ||||
chr2:144517337-144517590 | Rare:73; Clinvar:3; Clinvar (benign):4 | ||||
chr2:148020673-148021011 | Common:2; Rare:73 | ||||
chr2:148021571-148021646 | Rare:16 | ||||
chr2:151289619-151289671 | Rare:19 | ||||
chr2:152175699-152176008 | Common:1; Rare:78 | ||||
chr2:152717829-152717943 | Rare:47 | ||||
chr2:152717991-152718288 | Common:1; Rare:96 | ||||
chr2:152718500-152718643 | Rare:53 | ||||
chr2:156436287-156436410 | Common:1; Rare:36 | ||||
chr2:159616434-159616594 | Common:2; Rare:32 | ||||
chr2:159712390-159712577 | Common:2; Rare:76 | ||||
chr2:161308334-161308537 | Common:2; Rare:53 | ||||
chr2:162343908-162344167 | Rare:76 |