Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:49813835-49814168 | Common:1; Rare:140 | ||||
chr18:50266472-50266640 | Common:1; Rare:60 | ||||
chr18:50879012-50879228 | Common:4; Rare:73 | ||||
chr18:50967985-50968082 | Rare:44 | ||||
chr18:51030056-51030235 | Rare:58 | ||||
chr18:54357866-54357988 | Common:6; Rare:39 | ||||
chr18:55322147-55322500 | Common:1; Rare:62 | ||||
chr18:55401030-55401080 | Rare:10 | ||||
chr18:55401641-55401731 | Rare:18 | ||||
chr18:55585845-55585948 | Common:1; Rare:22 | ||||
chr18:55586062-55586184 | Common:1; Rare:42 | ||||
chr18:55588095-55588334 | Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr18:55589686-55589906 | Rare:62 | ||||
chr18:56651133-56651435 | Common:4; Rare:81 | ||||
chr18:56651460-56651705 | Common:4; Rare:55 |