Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:44435159-44435482 | Common:3; Rare:94 | ||||
chr13:44436719-44437028 | Common:3; Rare:89 | ||||
chr13:44576319-44576380 | Rare:16 | ||||
chr13:44989437-44989607 | Rare:64 | ||||
chr13:45120392-45120662 | Common:1; Rare:88 | ||||
chr13:45341037-45341609 | Common:4; Rare:258 | ||||
chr13:45464798-45465024 | Common:1; Rare:61 | ||||
chr13:45851682-45851883 | Common:1; Rare:42 | ||||
chr13:46052709-46052856 | Common:2; Rare:39 | ||||
chr13:46211811-46211969 | Common:2; Rare:53 | ||||
chr13:46387203-46387376 | Rare:47 | ||||
chr13:46553056-46553304 | Common:2; Rare:74 | ||||
chr13:46797104-46797362 | Common:3; Rare:86 | ||||
chr13:48001187-48001418 | Common:1; Rare:108; Clinvar:5; Clinvar (benign):11 | ||||
chr13:48037610-48037783 | Common:1; Rare:77 |