Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28719655-28720030 | Common:1; Rare:103 | ||||
chr17:28897613-28897732 | Common:1; Rare:41 | ||||
chr17:32350059-32350191 | Rare:74 | ||||
chr17:34961432-34961551 | Rare:50 | ||||
chr17:35242931-35243078 | Rare:46 | ||||
chr17:35587234-35587512 | Rare:75 | ||||
chr17:36534787-36534972 | Common:2; Rare:78 | ||||
chr17:36544806-36544942 | Common:1; Rare:44 | ||||
chr17:37406820-37406924 | Rare:38 | ||||
chr17:38825295-38825421 | Common:1; Rare:39 | ||||
chr17:38853696-38853888 | Common:3; Rare:78 | ||||
chr17:39637057-39637170 | Common:2; Rare:31 | ||||
chr17:41586308-41586458 | Rare:45; Clinvar:4 | ||||
chr17:41586649-41587199 | Common:6; Rare:169; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr17:41624139-41624642 | Common:7; Rare:204; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |