Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:59697665-59697852 | Common:1; Rare:51 | ||||
chr18:62186987-62187305 | Common:5; Rare:91 | ||||
chr18:63422407-63422681 | Common:2; Rare:76 | ||||
chr18:63476815-63476988 | Common:1; Rare:42 | ||||
chr18:63775311-63775443 | Common:1; Rare:29 | ||||
chr18:63777663-63777788 | Common:1; Rare:31 | ||||
chr18:63969981-63970133 | Common:2; Rare:26 | ||||
chr18:68715040-68715335 | Common:5; Rare:121 | ||||
chr18:70205659-70205763 | Common:2; Rare:46; Clinvar (benign):2 | ||||
chr18:79988421-79988628 | Common:3; Rare:77 | ||||
chr19:572374-572628 | Rare:142 | ||||
chr19:984207-984343 | Common:3; Rare:48 | ||||
chr19:1605405-1605665 | Common:3; Rare:101 | ||||
chr19:2328538-2328703 | Common:2; Rare:80 | ||||
chr19:4246905-4247090 | Common:2; Rare:56 |