Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31899452-31899558 | Common:1; Rare:19 | ||||
chr6:32116229-32116508 | Rare:38 | ||||
chr6:32169952-32170203 | Rare:55 | ||||
chr6:32180649-32181104 | Common:2; Rare:68 | ||||
chr6:32818278-32818310 | Common:1; Rare:9 | ||||
chr6:32894674-32894827 | Common:2; Rare:42 | ||||
chr6:33202961-33203327 | Rare:68 | ||||
chr6:33203329-33203625 | Common:1; Rare:59 | ||||
chr6:33210271-33210510 | Rare:43 | ||||
chr6:33249238-33249634 | Rare:119 | ||||
chr6:33250094-33250393 | Common:2; Rare:33 | ||||
chr6:33302211-33302252 | Rare:3 | ||||
chr6:33309107-33309422 | Common:1; Rare:42 | ||||
chr6:33403502-33403818 | Rare:63 | ||||
chr6:33432705-33432943 | Rare:42; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |