| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39655608-39655803 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771138-40771377 | Common:3; Rare:75 | ||||
| chr13:41060121-41060528 | Common:3; Rare:143 | ||||
| chr13:41060846-41061645 | Common:20; Rare:326 | ||||
| chr13:41061755-41061839 | Common:1; Rare:28 | ||||
| chr13:41132732-41132949 | Rare:57 | ||||
| chr13:41194466-41194716 | Common:2; Rare:57 | ||||
| chr13:41457298-41457552 | Common:2; Rare:75 | ||||
| chr13:43879467-43879627 | Rare:45 | ||||
| chr13:43879707-43879913 | Common:18; Rare:61 | ||||
| chr13:44989428-44989607 | Rare:69 | ||||
| chr13:45341040-45341609 | Common:4; Rare:258 | ||||
| chr13:45418314-45418548 | Rare:70 | ||||
| chr13:46052655-46052819 | Common:2; Rare:44 | ||||
| chr13:48001179-48001385 | Common:1; Rare:96; Clinvar:5; Clinvar (benign):11 |