Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:24160542-24160734 | Rare:52 | ||||
chr13:24512739-24512836 | Common:2; Rare:30 | ||||
chr13:26221787-26221972 | Rare:52 | ||||
chr13:27251225-27251626 | Common:8; Rare:126 | ||||
chr13:27424851-27424971 | Common:1; Rare:33 | ||||
chr13:27449973-27450230 | Common:3; Rare:75 | ||||
chr13:27450377-27450510 | Common:2; Rare:47 | ||||
chr13:27450518-27450670 | Common:2; Rare:60 | ||||
chr13:27620474-27620816 | Common:2; Rare:114 | ||||
chr13:28658941-28659187 | Rare:104; Clinvar (pathogenic):1 | ||||
chr13:28718797-28719159 | Common:1; Rare:93 | ||||
chr13:30306828-30307175 | Common:5; Rare:93 | ||||
chr13:30617263-30617406 | Rare:33 | ||||
chr13:30617460-30618046 | Common:1; Rare:189 | ||||
chr13:33285608-33285880 | Common:1; Rare:68 |