Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24705270-24705590 | Rare:76 | ||||
chr1:24724530-24724800 | Common:4; Rare:75 | ||||
chr1:24724890-24725300 | Common:1; Rare:80 | ||||
chr1:24725320-24725700 | Common:4; Rare:59 | ||||
chr1:24972170-24972560 | Common:2; Rare:76 | ||||
chr1:25022832-25023329 | Common:6; Rare:219 | ||||
chr1:25239711-25239928 | Common:3; Rare:53 | ||||
chr1:25566860-25567340 | Rare:120; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:25616497-25616827 | Common:6; Rare:108 | ||||
chr1:25699867-25700267 | Common:3; Rare:109 | ||||
chr1:25875713-25875839 | Rare:31 | ||||
chr1:25875862-25875998 | Common:2; Rare:43 | ||||
chr1:25921801-25922804 | Common:5; Rare:240 | ||||
chr1:25927150-25927780 | Rare:123 | ||||
chr1:25927800-25928100 | Common:1; Rare:41 |