Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:132887558-132887834 | Rare:79 | ||||
chr12:132956250-132956417 | Common:1; Rare:37 | ||||
chr12:133080725-133080960 | Rare:74 | ||||
chr13:19782927-19783082 | Common:2; Rare:56 | ||||
chr13:20773933-20774143 | Common:2; Rare:68 | ||||
chr13:21176500-21176708 | Common:1; Rare:94 | ||||
chr13:24512732-24512834 | Common:1; Rare:32 | ||||
chr13:24922795-24923117 | Common:2; Rare:111; Clinvar:1 | ||||
chr13:25301486-25301692 | Common:1; Rare:79 | ||||
chr13:26221791-26221990 | Rare:60 | ||||
chr13:27251289-27251632 | Common:4; Rare:98 | ||||
chr13:27424485-27424753 | Common:4; Rare:88 | ||||
chr13:27450130-27450230 | Common:3; Rare:29 | ||||
chr13:28658948-28659184 | Rare:103; Clinvar (pathogenic):1 | ||||
chr13:30307001-30307227 | Common:4; Rare:61 |