Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234612786-234613012 | Common:1; Rare:35 | ||||
chr1:234721975-234722251 | Common:2; Rare:54 | ||||
chr1:234724017-234724227 | Common:3; Rare:46 | ||||
chr1:234980759-234980885 | Rare:18 | ||||
chr1:236011883-236011925 | Rare:16 | ||||
chr1:236064258-236064398 | Common:1; Rare:15 | ||||
chr1:244451132-244451242 | Common:2; Rare:29 | ||||
chr1:244863702-244863875 | Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr1:244970949-244971110 | Rare:47 | ||||
chr10:241742-242043 | Common:4; Rare:101 | ||||
chr10:970319-970548 | Common:4; Rare:32 | ||||
chr10:5766494-5766921 | Common:3; Rare:95 | ||||
chr10:5945783-5946024 | Common:8; Rare:75 | ||||
chr10:6163635-6163889 | Common:7; Rare:90 | ||||
chr10:7795752-7795912 | Common:2; Rare:30 |