Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61362232-61362410 | Common:2; Rare:53; Clinvar:8; Clinvar (benign):1 | ||||
chr11:61392527-61392663 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429881-61430176 | Common:1; Rare:126; Clinvar:3; Clinvar (benign):6 | ||||
chr11:61481025-61481197 | Rare:31 | ||||
chr11:61792555-61792955 | Common:6; Rare:114 | ||||
chr11:61816760-61817094 | Rare:83 | ||||
chr11:61827693-61828344 | Common:1; Rare:131 | ||||
chr11:61840440-61840714 | Common:1; Rare:60 | ||||
chr11:61949606-61949821 | Common:2; Rare:35 | ||||
chr11:61967311-61967806 | Common:3; Rare:185; Clinvar:4 | ||||
chr11:62123771-62124121 | Common:6; Rare:88 | ||||
chr11:62337384-62337543 | Common:3; Rare:42 | ||||
chr11:62545674-62545916 | Common:1; Rare:47 | ||||
chr11:62591494-62591643 | Rare:69 | ||||
chr11:62601223-62601556 | Common:2; Rare:95 |