| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:109548486-109548828 | Common:5; Rare:121 | ||||
| chr1:110339149-110339447 | Common:1; Rare:83 | ||||
| chr1:110407632-110407901 | Common:4; Rare:116 | ||||
| chr1:110963880-110964028 | Rare:56 | ||||
| chr1:111140069-111140299 | Common:2; Rare:78 | ||||
| chr1:111199850-111200012 | Rare:28 | ||||
| chr1:111200629-111200955 | Common:2; Rare:62 | ||||
| chr1:111619464-111619900 | Common:2; Rare:122 | ||||
| chr1:111739374-111739551 | Common:1; Rare:44 | ||||
| chr1:112396009-112396281 | Common:1; Rare:84 | ||||
| chr1:112619101-112619221 | Rare:41 | ||||
| chr1:112619634-112619868 | Common:1; Rare:84 | ||||
| chr1:112956165-112956437 | Common:4; Rare:120; Clinvar:9; Clinvar (benign):3 | ||||
| chr1:113905016-113905380 | Common:4; Rare:105 | ||||
| chr1:114669999-114670225 | Common:1; Rare:69 |