| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39037486-39037856 | Common:1; Rare:118 | ||||
| chr13:39038058-39038426 | Common:1; Rare:94 | ||||
| chr13:40771138-40771407 | Common:3; Rare:81 | ||||
| chr13:40789370-40789601 | Common:2; Rare:76; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41061399-41061635 | Common:2; Rare:70 | ||||
| chr13:41132719-41132984 | Rare:72 | ||||
| chr13:43879691-43879894 | Common:18; Rare:61 | ||||
| chr13:44436769-44436997 | Common:2; Rare:71 | ||||
| chr13:44573248-44573532 | Common:1; Rare:96 | ||||
| chr13:44989432-44989607 | Rare:67 | ||||
| chr13:45120180-45120668 | Common:2; Rare:128 | ||||
| chr13:45341036-45341609 | Common:4; Rare:259 | ||||
| chr13:46052716-46052835 | Common:2; Rare:31 | ||||
| chr13:46182160-46182450 | Common:3; Rare:48 | ||||
| chr13:48001225-48001433 | Common:1; Rare:94; Clinvar:3; Clinvar (benign):6 |