| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111140036-111140263 | Common:1; Rare:81 | ||||
| chr1:111346537-111346655 | Rare:36 | ||||
| chr1:111473811-111473991 | Common:2; Rare:31 | ||||
| chr1:111619492-111619853 | Common:2; Rare:108 | ||||
| chr1:111739361-111739573 | Common:3; Rare:56 | ||||
| chr1:111739639-111739851 | Common:2; Rare:38 | ||||
| chr1:112396000-112396262 | Common:1; Rare:81 | ||||
| chr1:112619109-112619236 | Rare:45 | ||||
| chr1:112619634-112619856 | Common:1; Rare:77 | ||||
| chr1:112956145-112956393 | Common:4; Rare:104; Clinvar:10; Clinvar (benign):3 | ||||
| chr1:113073081-113073221 | Common:1; Rare:47 | ||||
| chr1:113905010-113905365 | Common:3; Rare:102 | ||||
| chr1:114152920-114153052 | Common:2; Rare:36 | ||||
| chr1:114581547-114581848 | Common:1; Rare:133 | ||||
| chr1:114716713-114716850 | Common:1; Rare:61; Clinvar:4; Clinvar (benign):1 |