Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:9102536-9102772 | Common:1; Rare:103; Clinvar:6; Clinvar (benign):2 | ||||
chr18:9136493-9136837 | Rare:133 | ||||
chr18:9914191-9914327 | Rare:59 | ||||
chr18:11851209-11851460 | Common:2; Rare:98 | ||||
chr18:11857463-11857755 | Common:1; Rare:61 | ||||
chr18:11908274-11908449 | Rare:53 | ||||
chr18:12407774-12407969 | Common:5; Rare:81 | ||||
chr18:12702658-12703084 | Common:3; Rare:171 | ||||
chr18:12884159-12884407 | Common:4; Rare:119 | ||||
chr18:12947703-12948098 | Common:3; Rare:107 | ||||
chr18:12991139-12991390 | Common:1; Rare:89 | ||||
chr18:13726439-13726729 | Common:3; Rare:112 | ||||
chr18:21111702-21111997 | Common:3; Rare:105 | ||||
chr18:21600625-21600852 | Rare:54 | ||||
chr18:21612187-21612428 | Common:1; Rare:73 |