Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:28659066-28659194 | Rare:55; Clinvar (pathogenic):1 | ||||
chr13:28718823-28719136 | Common:1; Rare:77 | ||||
chr13:29850647-29850693 | Rare:17 | ||||
chr13:30306813-30307187 | Common:7; Rare:99 | ||||
chr13:30307388-30307570 | Common:2; Rare:63 | ||||
chr13:30464235-30464338 | Rare:32 | ||||
chr13:30465760-30466132 | Common:1; Rare:115 | ||||
chr13:30617579-30618000 | Common:1; Rare:129 | ||||
chr13:31161841-31161872 | Rare:14 | ||||
chr13:31162341-31162454 | Common:1; Rare:27 | ||||
chr13:32315437-32315559 | Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
chr13:32538682-32538956 | Common:1; Rare:79 | ||||
chr13:33285662-33285887 | Rare:52 | ||||
chr13:33818042-33818222 | Rare:87 | ||||
chr13:36297768-36297909 | Common:1; Rare:51 |