| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111140036-111140305 | Common:2; Rare:93 | ||||
| chr1:111204351-111204703 | Common:1; Rare:83 | ||||
| chr1:111346526-111346670 | Common:1; Rare:39 | ||||
| chr1:111503626-111504001 | Common:2; Rare:66 | ||||
| chr1:111619575-111619929 | Common:2; Rare:110 | ||||
| chr1:111739348-111739551 | Common:1; Rare:51 | ||||
| chr1:112396013-112396265 | Common:1; Rare:79 | ||||
| chr1:112619101-112619236 | Rare:49 | ||||
| chr1:112619643-112619851 | Common:1; Rare:71 | ||||
| chr1:112956165-112956467 | Common:5; Rare:130; Clinvar:9; Clinvar (benign):3 | ||||
| chr1:113073095-113073238 | Common:1; Rare:54 | ||||
| chr1:113390192-113390531 | Common:1; Rare:84 | ||||
| chr1:113759129-113759173 | Rare:11 | ||||
| chr1:113812241-113812608 | Common:2; Rare:148 | ||||
| chr1:113905016-113905385 | Common:5; Rare:106 |