Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:11851276-11851456 | Common:2; Rare:62 | ||||
chr18:13726452-13726717 | Common:3; Rare:105 | ||||
chr18:22933807-22933902 | Common:1; Rare:37 | ||||
chr18:35290203-35290377 | Common:2; Rare:64 | ||||
chr18:36129282-36129493 | Common:1; Rare:62 | ||||
chr18:36129772-36129939 | Common:1; Rare:68 | ||||
chr18:36187371-36187573 | Common:4; Rare:69 | ||||
chr18:46098244-46098550 | Common:11; Rare:85; Clinvar (benign):5 | ||||
chr18:46104135-46104398 | Common:3; Rare:74; Clinvar (benign):1 | ||||
chr18:47150471-47150554 | Common:2; Rare:30 | ||||
chr18:49487196-49487355 | Common:3; Rare:61 | ||||
chr18:55665084-55665245 | Common:2; Rare:40 | ||||
chr18:63422370-63422660 | Common:1; Rare:78 | ||||
chr18:66604090-66604377 | Common:4; Rare:53 | ||||
chr18:68715061-68715253 | Common:3; Rare:88 |