Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31958899-31959182 | Rare:86; Clinvar:8 | ||||
chr6:32843986-32844087 | Rare:29; Clinvar:1 | ||||
chr6:32844334-32844447 | Rare:29 | ||||
chr6:32844582-32844840 | Common:1; Rare:54 | ||||
chr6:32853686-32853777 | Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
chr6:32854010-32854227 | Common:2; Rare:54 | ||||
chr6:33200656-33200920 | Common:2; Rare:81 | ||||
chr6:33271842-33272120 | Common:1; Rare:116 | ||||
chr6:33289209-33289287 | Rare:20 | ||||
chr6:34696738-34696975 | Common:1; Rare:55 | ||||
chr6:36874790-36874882 | Rare:33 | ||||
chr6:38639901-38639986 | Rare:23 | ||||
chr6:41072318-41072657 | Rare:103 | ||||
chr6:41921083-41921229 | Common:1; Rare:39 | ||||
chr6:42929226-42929556 | Common:3; Rare:91 |