Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110561615-110561938 | Common:5; Rare:108 | ||||
chr13:110615401-110615656 | Common:2; Rare:91 | ||||
chr13:110647205-110647418 | Common:2; Rare:65; Clinvar (benign):2 | ||||
chr13:110665705-110666021 | Common:1; Rare:48 | ||||
chr13:110713001-110713266 | Common:2; Rare:117 | ||||
chr13:110713481-110713662 | Common:2; Rare:76 | ||||
chr13:110715349-110715466 | Rare:41 | ||||
chr13:110715576-110715889 | Common:1; Rare:167 | ||||
chr13:110914356-110914740 | Common:7; Rare:164 | ||||
chr13:110915417-110915665 | Common:15; Rare:68 | ||||
chr13:111153620-111153955 | Common:3; Rare:137 | ||||
chr13:112588061-112588209 | Rare:42 | ||||
chr13:112689755-112690013 | Common:5; Rare:88 | ||||
chr13:112873248-112873459 | Common:3; Rare:16 | ||||
chr13:112968311-112968472 | Rare:41 |