Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:32298153-32298296 | Rare:23 | ||||
chr21:45347351-45347571 | Common:4; Rare:62 | ||||
chr22:20702657-20702847 | Common:2; Rare:42 | ||||
chr22:33921064-33921328 | Common:1; Rare:87 | ||||
chr22:37806187-37806403 | Common:2; Rare:46 | ||||
chr22:46052797-46052971 | Common:1; Rare:33 | ||||
chr3:41225501-41225758 | Rare:53; Clinvar (pathogenic):1 | ||||
chr3:41683032-41683285 | Common:2; Rare:55 | ||||
chr3:49357221-49357298 | Rare:18 | ||||
chr3:52693713-52694077 | Common:2; Rare:91 | ||||
chr3:75435046-75435366 | Common:3; Rare:115 | ||||
chr3:101676275-101676468 | Common:1; Rare:66 | ||||
chr3:107240582-107240739 | Rare:70 | ||||
chr3:112640330-112640519 | Common:1; Rare:37 | ||||
chr3:150408837-150408992 | Rare:47 |