| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:109667919-109668138 | Common:1; Rare:70 | ||||
| chr1:110339155-110339452 | Common:1; Rare:84 | ||||
| chr1:110391020-110391244 | Rare:41 | ||||
| chr1:110407621-110407840 | Common:3; Rare:97 | ||||
| chr1:111140046-111140286 | Common:2; Rare:82 | ||||
| chr1:111739341-111739704 | Common:3; Rare:100 | ||||
| chr1:112395963-112396258 | Common:2; Rare:95 | ||||
| chr1:112619091-112619199 | Rare:41 | ||||
| chr1:112619643-112619847 | Common:1; Rare:70 | ||||
| chr1:112956165-112956473 | Common:5; Rare:133; Clinvar:9; Clinvar (benign):3 | ||||
| chr1:113073095-113073221 | Common:1; Rare:45 | ||||
| chr1:113812273-113812579 | Common:2; Rare:121 | ||||
| chr1:113904850-113905385 | Common:7; Rare:163; Clinvar (benign):1 | ||||
| chr1:114695473-114695691 | Rare:52; Clinvar:1 | ||||
| chr1:114716732-114716862 | Common:1; Rare:58; Clinvar:4; Clinvar (benign):1 |