Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:924795-924950 | Rare:43 | ||||
chr1:925577-925753 | Common:1; Rare:54 | ||||
chr1:941549-941801 | Common:2; Rare:96 | ||||
chr1:941835-942176 | Common:1; Rare:165 | ||||
chr1:944819-945132 | Common:2; Rare:161 | ||||
chr1:959225-959452 | Common:1; Rare:118 | ||||
chr1:1000709-1001127 | Common:5; Rare:103 | ||||
chr1:1013367-1013576 | Common:4; Rare:66 | ||||
chr1:1013851-1014084 | Common:2; Rare:80; Clinvar (benign):1 | ||||
chr1:1231895-1232166 | Rare:89 | ||||
chr1:1273784-1274071 | Common:2; Rare:111 | ||||
chr1:1305659-1305908 | Common:1; Rare:82 | ||||
chr1:1307778-1307970 | Rare:42 | ||||
chr1:1308306-1308699 | Common:9; Rare:163 | ||||
chr1:1324594-1324820 | Common:3; Rare:124 |