| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:112619602-112619878 | Common:4; Rare:183 | ||||
| chr1:112674102-112674890 | Common:4; Rare:273 | ||||
| chr1:112707076-112707267 | Rare:113 | ||||
| chr1:112955880-112956100 | Rare:93; Clinvar:4 | ||||
| chr1:112956141-112956507 | Common:10; Rare:284; Clinvar:19; Clinvar (benign):6 | ||||
| chr1:113073083-113073255 | Common:2; Rare:127 | ||||
| chr1:113390163-113390556 | Common:3; Rare:199 | ||||
| chr1:113759423-113759593 | Common:6; Rare:91 | ||||
| chr1:113812210-113812690 | Common:5; Rare:327 | ||||
| chr1:113904793-113905442 | Common:14; Rare:361; Clinvar (benign):2 | ||||
| chr1:113928870-113929230 | Common:6; Rare:123 | ||||
| chr1:113929436-113929836 | Common:5; Rare:172 | ||||
| chr1:114511053-114511359 | Common:5; Rare:242 | ||||
| chr1:114581601-114581851 | Rare:198 | ||||
| chr1:114716701-114716876 | Common:2; Rare:150; Clinvar:8; Clinvar (benign):2 |