| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:226062493-226062835 | Rare:118 | ||||
| chr1:226186504-226186796 | Common:1; Rare:78 | ||||
| chr1:226309135-226309452 | Common:1; Rare:139 | ||||
| chr1:226309711-226309761 | Common:1; Rare:17 | ||||
| chr1:226407808-226408189 | Common:2; Rare:113 | ||||
| chr1:226870493-226870640 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr1:226939972-226940357 | Rare:135; Clinvar:3 | ||||
| chr1:227112347-227112575 | Rare:57 | ||||
| chr1:227318291-227318757 | Common:4; Rare:177 | ||||
| chr1:227735185-227735499 | Common:5; Rare:179 | ||||
| chr1:228082448-228082783 | Common:4; Rare:130 | ||||
| chr1:228083141-228083232 | Rare:24 | ||||
| chr1:228103296-228103450 | Common:1; Rare:54 | ||||
| chr1:228109223-228109475 | Rare:86 | ||||
| chr1:228139856-228140083 | Common:1; Rare:56 |