| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13123348-13123641 | Common:1; Rare:50 | ||||
| chr10:13123974-13124305 | Common:1; Rare:75; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr10:13591561-13591822 | Rare:51 | ||||
| chr10:14814816-14815069 | Common:1; Rare:53 | ||||
| chr10:14902252-14902498 | Rare:49 | ||||
| chr10:15098913-15099158 | Common:2; Rare:53 | ||||
| chr10:15259469-15259672 | Common:1; Rare:26 | ||||
| chr10:16712990-16713252 | Rare:46 | ||||
| chr10:17439300-17439537 | Common:2; Rare:35 | ||||
| chr10:18512916-18513150 | Common:3; Rare:59 | ||||
| chr10:19708446-19708642 | Common:1; Rare:6 | ||||
| chr10:19789656-19789844 | Rare:45 | ||||
| chr10:19869278-19869531 | Common:4; Rare:41 | ||||
| chr10:19913486-19913757 | Rare:54 | ||||
| chr10:19971273-19971475 | Common:5; Rare:37 |