Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23531291-23531467 | Common:2; Rare:21 | ||||
chr1:23559440-23559643 | Common:1; Rare:90 | ||||
chr1:23691671-23691918 | Common:6; Rare:94; Clinvar:2; Clinvar (benign):3 | ||||
chr1:23692245-23692320 | Rare:23 | ||||
chr1:23692335-23692760 | Common:4; Rare:122; Clinvar:1; Clinvar (benign):4 | ||||
chr1:23778239-23778507 | Common:9; Rare:138 | ||||
chr1:23791857-23792013 | Rare:32 | ||||
chr1:23825382-23825544 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:23959631-23959975 | Common:2; Rare:83 | ||||
chr1:23980246-23980447 | Rare:65 | ||||
chr1:24187239-24187452 | Common:8; Rare:63 | ||||
chr1:24415464-24415827 | Common:3; Rare:88 | ||||
chr1:24502637-24502934 | Rare:92 | ||||
chr1:24556032-24556121 | Common:2; Rare:30 | ||||
chr1:24642890-24643363 | Common:2; Rare:154 |