| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111739374-111739551 | Common:1; Rare:44 | ||||
| chr1:112619099-112619242 | Rare:51 | ||||
| chr1:112619642-112619877 | Common:2; Rare:84 | ||||
| chr1:112956169-112956467 | Common:5; Rare:129; Clinvar:9; Clinvar (benign):3 | ||||
| chr1:113073068-113073255 | Common:1; Rare:78 | ||||
| chr1:113812258-113812623 | Common:3; Rare:141 | ||||
| chr1:113904785-113905445 | Common:7; Rare:189; Clinvar (benign):1 | ||||
| chr1:113929263-113929376 | Common:1; Rare:31 | ||||
| chr1:114581578-114581832 | Common:1; Rare:113 | ||||
| chr1:116570925-116571197 | Common:3; Rare:77 | ||||
| chr1:117060060-117060359 | Common:6; Rare:80 | ||||
| chr1:117367323-117367563 | Common:5; Rare:81 | ||||
| chr1:117929546-117929863 | Common:4; Rare:95 | ||||
| chr1:119140584-119140768 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
| chr1:119368477-119368785 | Common:1; Rare:44 |