| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111140041-111140286 | Common:2; Rare:83 | ||||
| chr1:111619606-111619932 | Common:2; Rare:105 | ||||
| chr1:111739316-111739517 | Common:1; Rare:54 | ||||
| chr1:111755533-111755766 | Common:4; Rare:87 | ||||
| chr1:112619683-112619878 | Common:2; Rare:72 | ||||
| chr1:112956029-112956442 | Common:4; Rare:152; Clinvar:12; Clinvar (benign):3 | ||||
| chr1:113073085-113073231 | Common:1; Rare:50 | ||||
| chr1:113390201-113390515 | Common:1; Rare:77 | ||||
| chr1:113759461-113759604 | Common:2; Rare:45 | ||||
| chr1:113904793-113905375 | Common:6; Rare:168; Clinvar (benign):1 | ||||
| chr1:113929512-113929671 | Common:1; Rare:46 | ||||
| chr1:114511069-114511278 | Common:1; Rare:94 | ||||
| chr1:114581573-114581843 | Common:1; Rare:118 | ||||
| chr1:114716112-114716423 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr1:114716658-114716985 | Common:4; Rare:125; Clinvar:5; Clinvar (benign):3 |