| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102117871-102118022 | Common:1; Rare:30 | ||||
| chr10:102119238-102119939 | Common:4; Rare:133 | ||||
| chr10:102133532-102133864 | Common:1; Rare:82 | ||||
| chr10:102133916-102134133 | Rare:53 | ||||
| chr10:102153147-102153281 | Common:2; Rare:28 | ||||
| chr10:102153561-102153617 | Rare:10 | ||||
| chr10:102246373-102246634 | Common:1; Rare:39 | ||||
| chr10:102399556-102399662 | Rare:38; Clinvar (benign):1 | ||||
| chr10:102401830-102402046 | Common:2; Rare:66; Clinvar (benign):2 | ||||
| chr10:102422165-102422332 | Rare:32 | ||||
| chr10:102422683-102422942 | Rare:75 | ||||
| chr10:102431833-102432047 | Common:5; Rare:42 | ||||
| chr10:102449699-102449991 | Common:1; Rare:59 | ||||
| chr10:102450158-102450226 | Rare:12 | ||||
| chr10:102450323-102450840 | Common:1; Rare:200 |