| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:24466397-24466536 | Rare:25 | ||||
| chr10:24952561-24952923 | Common:4; Rare:113 | ||||
| chr10:27100431-27100676 | Common:4; Rare:63; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154310-27154495 | Rare:51 | ||||
| chr10:27155165-27155375 | Common:4; Rare:69; Clinvar:5; Clinvar (benign):4 | ||||
| chr10:27242058-27242221 | Common:1; Rare:69 | ||||
| chr10:28532430-28532817 | Common:5; Rare:143 | ||||
| chr10:30059501-30059657 | Common:1; Rare:60 | ||||
| chr10:31031848-31032052 | Common:2; Rare:83 | ||||
| chr10:31032382-31032506 | Common:4; Rare:29 | ||||
| chr10:31319021-31319289 | Common:2; Rare:75 | ||||
| chr10:31928748-31929126 | Common:4; Rare:126 | ||||
| chr10:32056368-32056482 | Common:1; Rare:48 | ||||
| chr10:32378724-32378890 | Common:1; Rare:23 | ||||
| chr10:32446044-32446255 | Common:1; Rare:96 |