| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13099877-13100247 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:13300033-13300149 | Rare:47; Clinvar:1 | ||||
| chr10:13348006-13348370 | Rare:123 | ||||
| chr10:13586775-13587051 | Common:3; Rare:96 | ||||
| chr10:14604247-14604553 | Common:5; Rare:133 | ||||
| chr10:14837948-14838398 | Common:4; Rare:138 | ||||
| chr10:14878597-14878904 | Common:2; Rare:99 | ||||
| chr10:14954023-14954172 | Rare:48 | ||||
| chr10:14954322-14954439 | Common:2; Rare:25 | ||||
| chr10:14959267-14959412 | Common:1; Rare:43 | ||||
| chr10:14959557-14959678 | Rare:42 | ||||
| chr10:15088724-15088923 | Common:1; Rare:86 | ||||
| chr10:15097285-15097409 | Common:2; Rare:64 | ||||
| chr10:15860442-15860623 | Rare:48 | ||||
| chr10:16817349-16817755 | Common:4; Rare:147 |