Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:44873613-44874040 | Common:8; Rare:173 | ||||
chr22:17628712-17628872 | Common:1; Rare:54 | ||||
chr22:19432303-19432557 | Common:3; Rare:100 | ||||
chr22:19479158-19479466 | Common:4; Rare:102 | ||||
chr22:24555837-24556038 | Rare:65 | ||||
chr22:26512452-26512529 | Common:1; Rare:34 | ||||
chr22:29267969-29268328 | Common:2; Rare:105 | ||||
chr22:29767053-29767394 | Common:4; Rare:105 | ||||
chr22:37849316-37849446 | Rare:74 | ||||
chr22:41621018-41621362 | Common:7; Rare:129 | ||||
chr22:42090737-42090941 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
chr22:42649322-42649482 | Common:1; Rare:64 | ||||
chr22:50783628-50783844 | Common:1; Rare:64 | ||||
chr3:9363025-9363069 | Rare:16 | ||||
chr3:9792979-9793109 | Common:2; Rare:58 |