Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19776378-19776626 | Common:2; Rare:70 | ||||
chr19:20423682-20423756 | Common:1; Rare:20 | ||||
chr19:23274186-23274391 | Common:2; Rare:51 | ||||
chr19:27793370-27793477 | Common:1; Rare:28 | ||||
chr19:27793678-27794066 | Common:1; Rare:97 | ||||
chr19:30226653-30226823 | Rare:32 | ||||
chr19:35131804-35131999 | Rare:58 | ||||
chr19:36142725-36142951 | Rare:53 | ||||
chr19:39403749-39403879 | Rare:21 | ||||
chr19:39409625-39409785 | Rare:39 | ||||
chr19:40403755-40404051 | Common:2; Rare:87; Clinvar:3; Clinvar (benign):4 | ||||
chr19:40414761-40414848 | Rare:18 | ||||
chr19:40736365-40736492 | Rare:16 | ||||
chr19:40810744-40810962 | Common:2; Rare:58 | ||||
chr19:40812107-40812333 | Common:3; Rare:42 |