Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:135054784-135054990 | Common:6; Rare:62 | ||||
chr6:135497612-135497810 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
chr6:136289767-136290024 | Common:1; Rare:112 | ||||
chr6:137219330-137219627 | Common:5; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
chr6:137867047-137867365 | Rare:72 | ||||
chr6:138545627-138545871 | Common:1; Rare:49 | ||||
chr6:138773646-138773813 | Common:3; Rare:77 | ||||
chr6:142147135-142147289 | Rare:57 | ||||
chr6:143060700-143060919 | Common:7; Rare:73 | ||||
chr6:143450654-143450929 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
chr6:144285219-144285382 | Common:2; Rare:42 | ||||
chr6:145814664-145814921 | Common:1; Rare:115 | ||||
chr6:149749647-149749796 | Rare:85 | ||||
chr6:149963819-149964007 | Common:1; Rare:54 | ||||
chr6:150866330-150866584 | Rare:95 |