Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:132887558-132887804 | Rare:72 | ||||
chr12:132956271-132956370 | Common:1; Rare:25 | ||||
chr12:133130435-133130627 | Common:3; Rare:58 | ||||
chr13:19863633-19863877 | Common:2; Rare:93 | ||||
chr13:21140392-21140622 | Rare:108 | ||||
chr13:21176510-21176708 | Common:1; Rare:91 | ||||
chr13:23889321-23889586 | Common:1; Rare:90 | ||||
chr13:24512739-24512834 | Common:1; Rare:29 | ||||
chr13:24922801-24923002 | Rare:55; Clinvar:1 | ||||
chr13:25301492-25301721 | Common:1; Rare:85 | ||||
chr13:26221791-26221953 | Rare:46 | ||||
chr13:27251251-27251608 | Common:4; Rare:106 | ||||
chr13:27450392-27450643 | Common:4; Rare:101 | ||||
chr13:27620493-27620799 | Common:2; Rare:98 | ||||
chr13:28658952-28659180 | Rare:102; Clinvar (pathogenic):1 |