Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:143943847-143944112 | Rare:106 | ||||
chr8:144060678-144060820 | Rare:42 | ||||
chr8:144078548-144078722 | Common:1; Rare:51 | ||||
chr8:144082503-144082689 | Common:2; Rare:65 | ||||
chr8:144095781-144095855 | Rare:23 | ||||
chr8:144095977-144096211 | Rare:98; Clinvar (benign):1 | ||||
chr8:144103686-144103872 | Common:1; Rare:68 | ||||
chr8:144104215-144104550 | Common:1; Rare:118 | ||||
chr8:144291358-144291647 | Common:1; Rare:93 | ||||
chr8:144394118-144394265 | Rare:55 | ||||
chr8:144398968-144399233 | Rare:111 | ||||
chr8:144413548-144413719 | Rare:51; Clinvar:1 | ||||
chr8:144428497-144428688 | Common:2; Rare:73 | ||||
chr8:144465351-144465496 | Common:3; Rare:58 | ||||
chr8:144500923-144501173 | Rare:123 |