| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:24607504-24607815 | Rare:88 | ||||
| chr10:24722584-24722842 | Rare:63 | ||||
| chr10:24723156-24723447 | Common:2; Rare:82 | ||||
| chr10:24952270-24952382 | Rare:22 | ||||
| chr10:24952561-24952904 | Common:4; Rare:108 | ||||
| chr10:25016420-25016685 | Common:8; Rare:101 | ||||
| chr10:26438135-26438414 | Common:2; Rare:67 | ||||
| chr10:27100409-27100603 | Common:3; Rare:55; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154290-27154480 | Rare:50 | ||||
| chr10:27155161-27155429 | Common:7; Rare:114; Clinvar:5; Clinvar (benign):7 | ||||
| chr10:27240457-27240889 | Common:2; Rare:123 | ||||
| chr10:27242058-27242235 | Common:1; Rare:76 | ||||
| chr10:27504057-27504356 | Rare:143; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:28532695-28532896 | Common:1; Rare:73 | ||||
| chr10:28533002-28533281 | Rare:112 |