Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:32315384-32315552 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
chr13:32586250-32586582 | Common:2; Rare:100 | ||||
chr13:33285693-33285887 | Rare:43 | ||||
chr13:35855614-35855813 | Common:1; Rare:38 | ||||
chr13:36346301-36346459 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
chr13:36999292-36999465 | Rare:66 | ||||
chr13:37059600-37059773 | Common:1; Rare:60 | ||||
chr13:38350252-38350584 | Common:2; Rare:84 | ||||
chr13:39038111-39038422 | Common:1; Rare:79 | ||||
chr13:40771130-40771439 | Common:3; Rare:93 | ||||
chr13:40789352-40789609 | Common:2; Rare:86; Clinvar:5; Clinvar (benign):2 | ||||
chr13:41061356-41061598 | Common:2; Rare:71 | ||||
chr13:41311142-41311316 | Rare:73 | ||||
chr13:41457283-41457547 | Common:2; Rare:77 | ||||
chr13:42992184-42992367 | Common:2; Rare:38 |