Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10399749-10399861 | Common:2; Rare:31 | ||||
chr1:10415527-10415685 | Rare:22 | ||||
chr1:10430309-10430522 | Common:6; Rare:61 | ||||
chr1:10430592-10430802 | Common:5; Rare:75 | ||||
chr1:10431075-10431272 | Common:2; Rare:50 | ||||
chr1:10472427-10472841 | Rare:99 | ||||
chr1:10474836-10475044 | Rare:81; Clinvar:4; Clinvar (benign):1 | ||||
chr1:10475390-10475419 | Common:1; Rare:6 | ||||
chr1:10694750-10694921 | Rare:53 | ||||
chr1:10796632-10796876 | Common:2; Rare:68 | ||||
chr1:11012225-11012745 | Common:3; Rare:145; Clinvar:4; Clinvar (benign):1 | ||||
chr1:11012991-11013122 | Rare:47 | ||||
chr1:11059912-11060259 | Common:2; Rare:106 | ||||
chr1:11060268-11060474 | Common:2; Rare:60 | ||||
chr1:11099298-11099512 | Rare:50 |