| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:45594496-45594678 | Common:1; Rare:56 | ||||
| chr10:45594769-45595069 | Common:2; Rare:112 | ||||
| chr10:45672218-45672392 | Rare:28 | ||||
| chr10:45672424-45673011 | Common:1; Rare:189 | ||||
| chr10:45727162-45727308 | Common:1; Rare:63 | ||||
| chr10:45972339-45972504 | Common:1; Rare:47 | ||||
| chr10:46030464-46030808 | Common:1; Rare:93 | ||||
| chr10:48306322-48306777 | Common:2; Rare:170 | ||||
| chr10:48306905-48307011 | Rare:33 | ||||
| chr10:48656262-48656533 | Common:3; Rare:70 | ||||
| chr10:48684591-48684931 | Common:2; Rare:75 | ||||
| chr10:48684933-48685613 | Common:4; Rare:158 | ||||
| chr10:49188320-49188552 | Common:2; Rare:59 | ||||
| chr10:49538724-49538881 | Common:5; Rare:42 | ||||
| chr10:49538977-49539240 | Common:3; Rare:89; Clinvar:3; Clinvar (benign):2 |