| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:40789338-40789615 | Common:2; Rare:94; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41132808-41132949 | Rare:31 | ||||
| chr13:41263552-41263736 | Rare:38 | ||||
| chr13:43023041-43023188 | Common:2; Rare:32 | ||||
| chr13:43023476-43023633 | Common:1; Rare:54 | ||||
| chr13:43879738-43879867 | Common:16; Rare:48 | ||||
| chr13:44989428-44989628 | Rare:78 | ||||
| chr13:45120392-45120570 | Common:1; Rare:58 | ||||
| chr13:45341040-45341521 | Common:4; Rare:232 | ||||
| chr13:45464753-45464995 | Common:1; Rare:60 | ||||
| chr13:46052718-46052842 | Common:2; Rare:33 | ||||
| chr13:46182135-46182391 | Common:3; Rare:43 | ||||
| chr13:46797104-46797262 | Common:2; Rare:53 | ||||
| chr13:48493017-48493229 | Common:2; Rare:24 | ||||
| chr13:48533038-48533171 | Common:2; Rare:43 |