Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23865470-23865870 | Common:6; Rare:220; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):6 | ||||
chr1:23888120-23888350 | Common:3; Rare:43 | ||||
chr1:23888260-23888383 | Common:1; Rare:17 | ||||
chr1:23888360-23888800 | Common:5; Rare:95 | ||||
chr1:23889133-23889316 | Common:5; Rare:28 | ||||
chr1:23903556-23903956 | Common:6; Rare:94 | ||||
chr1:23904819-23905121 | Common:2; Rare:55 | ||||
chr1:23906791-23906975 | Common:2; Rare:21 | ||||
chr1:23907744-23908144 | Common:3; Rare:80 | ||||
chr1:23908793-23909256 | Rare:241 | ||||
chr1:23909425-23909854 | Common:10; Rare:208 | ||||
chr1:23910270-23910442 | Common:2; Rare:22 | ||||
chr1:23910620-23911229 | Common:7; Rare:226 | ||||
chr1:23911583-23911983 | Common:1; Rare:124 | ||||
chr1:23912038-23912382 | Common:1; Rare:61 |