Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:21740759-21740802 | Rare:13 | ||||
chr18:31206872-31206928 | Rare:12 | ||||
chr18:31206958-31207270 | Common:3; Rare:60 | ||||
chr18:31419715-31419919 | Common:2; Rare:32 | ||||
chr18:31449132-31449368 | Rare:38 | ||||
chr18:31449868-31450243 | Common:3; Rare:59 | ||||
chr18:31453311-31453570 | Common:3; Rare:40 | ||||
chr18:31724629-31724680 | Rare:7 | ||||
chr18:35412649-35412856 | Rare:37 | ||||
chr18:35478559-35478808 | Rare:33 | ||||
chr18:39313960-39314240 | Common:1; Rare:52 | ||||
chr18:46087130-46087452 | Rare:72; Clinvar (pathogenic):2 | ||||
chr18:46174861-46174901 | Rare:10 | ||||
chr18:46868344-46868660 | Rare:67 | ||||
chr18:48036799-48037078 | Common:2; Rare:46 |