Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:45894653-45895011 | Common:3; Rare:126; Clinvar:3; Clinvar (benign):2 | ||||
chr20:45899470-45899671 | Rare:68 | ||||
chr20:49289214-49289256 | Rare:4 | ||||
chr20:50292611-50292765 | Common:2; Rare:34 | ||||
chr21:46003136-46003677 | Common:7; Rare:207; Clinvar:27; Clinvar (benign):23 | ||||
chr21:46125460-46126236 | Common:7; Rare:406; Clinvar:61; Clinvar (benign):35; Clinvar (pathogenic):6 | ||||
chr21:46130630-46130684 | Common:1; Rare:21 | ||||
chr22:20206227-20206403 | Common:2; Rare:42 | ||||
chr22:20702617-20702851 | Common:2; Rare:54 | ||||
chr22:21939611-21939763 | Rare:38 | ||||
chr22:23717323-23717495 | Rare:57 | ||||
chr22:36293840-36294156 | Common:5; Rare:95; Clinvar:1; Clinvar (benign):5 | ||||
chr22:37806111-37806412 | Common:4; Rare:73 | ||||
chr22:50526968-50527185 | Rare:71; Clinvar (pathogenic):1 | ||||
chr3:40453161-40453444 | Common:6; Rare:64 |