Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:185761572-185761751 | Common:1; Rare:27 | ||||
chr4:186723759-186723917 | Common:5; Rare:65 | ||||
chr4:189940626-189941048 | Common:16; Rare:158 | ||||
chr5:218108-218415 | Common:4; Rare:122; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr5:443088-443281 | Common:9; Rare:89 | ||||
chr5:612211-612363 | Rare:60 | ||||
chr5:693286-693596 | Common:6; Rare:91 | ||||
chr5:892647-892854 | Common:5; Rare:69 | ||||
chr5:1799778-1799988 | Common:8; Rare:99 | ||||
chr5:1801300-1801455 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
chr5:5422311-5422677 | Common:3; Rare:124 | ||||
chr5:6378479-6378699 | Rare:93 | ||||
chr5:6632941-6633410 | Common:10; Rare:151; Clinvar:10; Clinvar (benign):6 | ||||
chr5:7869000-7869209 | Common:2; Rare:106; Clinvar (benign):1 | ||||
chr5:9546001-9546351 | Common:9; Rare:88 |