Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47553090-47553356 | Common:2; Rare:91 | ||||
chr11:47565478-47565650 | Common:3; Rare:35 | ||||
chr11:47578940-47579097 | Rare:82; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr11:57324905-57325075 | Common:1; Rare:59 | ||||
chr11:57530682-57530863 | Common:1; Rare:45 | ||||
chr11:57712184-57712624 | Common:9; Rare:146 | ||||
chr11:58577554-58577781 | Rare:40 | ||||
chr11:58578354-58578490 | Common:2; Rare:50 | ||||
chr11:59142672-59142951 | Common:1; Rare:50 | ||||
chr11:59668991-59669312 | Rare:109 | ||||
chr11:60841883-60842141 | Common:2; Rare:91 | ||||
chr11:60906507-60906737 | Rare:62 | ||||
chr11:60913835-60914235 | Common:1; Rare:83 | ||||
chr11:60952366-60952516 | Rare:29 | ||||
chr11:61333026-61333261 | Rare:79 |