Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19251505-19251843 | Common:6; Rare:111 | ||||
chr1:19312012-19312333 | Common:8; Rare:153 | ||||
chr1:21345476-21345655 | Common:1; Rare:70 | ||||
chr1:21669310-21669480 | Rare:51 | ||||
chr1:21875634-21875899 | Common:3; Rare:87; Clinvar:3; Clinvar (benign):2 | ||||
chr1:23369789-23369938 | Rare:27 | ||||
chr1:23558933-23559171 | Common:4; Rare:115 | ||||
chr1:23559374-23559671 | Common:2; Rare:127 | ||||
chr1:23691729-23691826 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23778281-23778572 | Common:10; Rare:127 | ||||
chr1:23791075-23791231 | Rare:45 | ||||
chr1:23868280-23868430 | Common:4; Rare:48; Clinvar:1; Clinvar (benign):3 | ||||
chr1:23959608-23959854 | Common:2; Rare:65 | ||||
chr1:23980189-23980542 | Common:1; Rare:95 | ||||
chr1:24642973-24643346 | Common:2; Rare:117 |