| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:108559830-108560180 | Common:3; Rare:125 | ||||
| chr1:108692175-108692348 | Common:2; Rare:62 | ||||
| chr1:108746447-108746740 | Common:2; Rare:107 | ||||
| chr1:108817118-108817274 | Rare:42 | ||||
| chr1:108852430-108852902 | Common:4; Rare:168 | ||||
| chr1:108876820-108877029 | Common:1; Rare:58; Clinvar:2 | ||||
| chr1:108877156-108877556 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:108963367-108963645 | Common:1; Rare:96 | ||||
| chr1:109041085-109041238 | Common:1; Rare:32 | ||||
| chr1:109042029-109042415 | Common:5; Rare:103 | ||||
| chr1:109075926-109076268 | Rare:107 | ||||
| chr1:109090605-109090768 | Common:4; Rare:27 | ||||
| chr1:109091108-109091238 | Common:1; Rare:41 | ||||
| chr1:109111984-109112637 | Common:6; Rare:146 | ||||
| chr1:109112731-109112931 | Common:2; Rare:50 |