Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:32142399-32142714 | Common:8; Rare:126 | ||||
chr17:32341904-32341961 | Rare:17 | ||||
chr17:32350027-32350228 | Rare:106 | ||||
chr17:32876499-32876776 | Rare:95 | ||||
chr17:34255073-34255420 | Rare:97 | ||||
chr17:34961444-34961575 | Common:1; Rare:62 | ||||
chr17:34980420-34980618 | Common:4; Rare:59 | ||||
chr17:34981080-34981243 | Common:1; Rare:31 | ||||
chr17:35063637-35063836 | Rare:33 | ||||
chr17:35089098-35089436 | Common:5; Rare:82 | ||||
chr17:35119725-35119983 | Rare:91; Clinvar:4; Clinvar (benign):1 | ||||
chr17:35242900-35243124 | Rare:78 | ||||
chr17:35373611-35373771 | Common:3; Rare:34 | ||||
chr17:35432328-35432704 | Common:3; Rare:64 | ||||
chr17:35578411-35578715 | Common:2; Rare:75; Clinvar:4; Clinvar (benign):2 |