| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:43880041-43880060 | Rare:2 | ||||
| chr13:44989443-44989610 | Rare:62 | ||||
| chr13:45120377-45120532 | Common:2; Rare:46 | ||||
| chr13:45341040-45341570 | Common:4; Rare:243 | ||||
| chr13:45464768-45465015 | Common:1; Rare:63 | ||||
| chr13:46052696-46052861 | Common:2; Rare:47 | ||||
| chr13:46182113-46182422 | Common:3; Rare:56 | ||||
| chr13:46387167-46387396 | Rare:62 | ||||
| chr13:46387410-46387578 | Common:1; Rare:35 | ||||
| chr13:46389478-46389714 | Common:1; Rare:34 | ||||
| chr13:46390068-46390141 | Rare:12 | ||||
| chr13:46390148-46390310 | Common:1; Rare:21 | ||||
| chr13:46553015-46553187 | Common:2; Rare:66 | ||||
| chr13:46797104-46797315 | Common:3; Rare:75 | ||||
| chr13:48001264-48001376 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):2 |