Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:43879489-43879606 | Rare:34 | ||||
chr13:44989440-44989597 | Rare:60 | ||||
chr13:45120379-45120531 | Common:2; Rare:44 | ||||
chr13:45341104-45341410 | Common:4; Rare:156 | ||||
chr13:46052718-46052871 | Common:2; Rare:43 | ||||
chr13:48303517-48303887 | Rare:107; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:49247806-49248029 | Rare:63 | ||||
chr13:49443992-49444373 | Common:1; Rare:123 | ||||
chr13:49936274-49936596 | Rare:98 | ||||
chr13:49997006-49997092 | Rare:27 | ||||
chr13:50081980-50082267 | Common:1; Rare:79 | ||||
chr13:51452142-51452383 | Common:3; Rare:68 | ||||
chr13:51804113-51804296 | Common:2; Rare:53 | ||||
chr13:52455334-52455613 | Common:3; Rare:106 | ||||
chr13:60163821-60164112 | Common:2; Rare:74 |