Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23531305-23531522 | Common:3; Rare:28 | ||||
chr1:23559411-23559684 | Common:2; Rare:117 | ||||
chr1:23691645-23691897 | Common:5; Rare:89; Clinvar:2; Clinvar (benign):3 | ||||
chr1:23743297-23743510 | Rare:81 | ||||
chr1:23778247-23778578 | Common:10; Rare:146 | ||||
chr1:23791066-23791231 | Rare:51 | ||||
chr1:23800723-23800959 | Common:1; Rare:84 | ||||
chr1:23825398-23825550 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959095-23959304 | Common:3; Rare:38 | ||||
chr1:23959607-23959877 | Common:2; Rare:75 | ||||
chr1:23960053-23960086 | Rare:13 | ||||
chr1:23979917-23980011 | Common:1; Rare:37 | ||||
chr1:23980189-23980605 | Common:1; Rare:114 | ||||
chr1:24413696-24413849 | Common:1; Rare:33 | ||||
chr1:24415566-24415834 | Common:2; Rare:70 |