Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46360525-46360733 | Rare:50; Clinvar (benign):1 | ||||
chr2:46369530-46369871 | Common:1; Rare:82; Clinvar (benign):1 | ||||
chr2:46382174-46382591 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):3 | ||||
chr2:47335017-47335323 | Rare:67 | ||||
chr2:47795815-47795995 | Common:3; Rare:57; Clinvar:18; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
chr2:47906467-47906817 | Common:2; Rare:129 | ||||
chr2:58113141-58113278 | Rare:40 | ||||
chr2:58118705-58118805 | Common:1; Rare:34 | ||||
chr2:61188981-61189261 | Common:1; Rare:71 | ||||
chr2:61880284-61880588 | Common:1; Rare:68 | ||||
chr2:62441904-62442158 | Common:2; Rare:49 | ||||
chr2:62443401-62443767 | Common:4; Rare:65 | ||||
chr2:62443954-62444240 | Common:2; Rare:55 | ||||
chr2:64211160-64211316 | Rare:34 | ||||
chr2:65567408-65567507 | Common:1; Rare:15 |