| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:22316225-22316518 | Common:2; Rare:135 | ||||
| chr10:22321348-22321624 | Rare:92 | ||||
| chr10:22325513-22325671 | Rare:69 | ||||
| chr10:24208719-24209297 | Common:3; Rare:169 | ||||
| chr10:24466428-24466560 | Rare:25 | ||||
| chr10:24722586-24722842 | Rare:63 | ||||
| chr10:24723161-24723429 | Common:2; Rare:73 | ||||
| chr10:24952340-24952376 | Rare:7 | ||||
| chr10:24952566-24952894 | Common:4; Rare:99 | ||||
| chr10:25016473-25016677 | Common:4; Rare:81 | ||||
| chr10:26438211-26438393 | Common:1; Rare:36 | ||||
| chr10:27100413-27100582 | Common:3; Rare:50; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154310-27154521 | Rare:62 | ||||
| chr10:27155154-27155371 | Common:3; Rare:71; Clinvar:5; Clinvar (benign):3 | ||||
| chr10:27240466-27240896 | Common:2; Rare:124 |