Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:110407604-110407805 | Common:2; Rare:89 | ||||
chr1:110407922-110407987 | Rare:15 | ||||
chr1:111139174-111139512 | Common:2; Rare:69 | ||||
chr1:111140041-111140286 | Common:2; Rare:83 | ||||
chr1:111200127-111200326 | Common:3; Rare:29 | ||||
chr1:111204345-111204553 | Rare:50 | ||||
chr1:111739380-111739689 | Common:3; Rare:86 | ||||
chr1:112619101-112619236 | Rare:49 | ||||
chr1:112619643-112619722 | Rare:25 | ||||
chr1:112619731-112619868 | Common:1; Rare:53 | ||||
chr1:112703011-112703370 | Common:1; Rare:69 | ||||
chr1:112707080-112707228 | Rare:50 | ||||
chr1:112956193-112956521 | Common:5; Rare:136; Clinvar:8; Clinvar (benign):3 | ||||
chr1:113073111-113073265 | Common:1; Rare:66 | ||||
chr1:113390155-113390562 | Common:2; Rare:107 |