Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47553078-47553357 | Common:2; Rare:97 | ||||
chr11:47565489-47565646 | Common:3; Rare:32 | ||||
chr11:47578967-47579094 | Rare:64; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr11:47642461-47642799 | Rare:123 | ||||
chr11:57324883-57325173 | Common:1; Rare:96 | ||||
chr11:57712165-57712643 | Common:9; Rare:161 | ||||
chr11:57761609-57762044 | Common:3; Rare:84 | ||||
chr11:57781427-57781624 | Rare:34 | ||||
chr11:58578248-58578512 | Common:3; Rare:95 | ||||
chr11:59142705-59142879 | Rare:24 | ||||
chr11:60906434-60906664 | Rare:55 | ||||
chr11:60914057-60914232 | Common:1; Rare:51 | ||||
chr11:61161408-61161732 | Common:1; Rare:89 | ||||
chr11:61333033-61333275 | Common:1; Rare:89 | ||||
chr11:61361842-61362026 | Common:1; Rare:43 |