| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37000736-37000822 | Rare:35; Clinvar (pathogenic):1 | ||||
| chr13:37059560-37059751 | Common:1; Rare:64 | ||||
| chr13:38349544-38349948 | Common:4; Rare:140; Clinvar (pathogenic):1 | ||||
| chr13:38350215-38350345 | Rare:45 | ||||
| chr13:39037296-39037540 | Common:1; Rare:57 | ||||
| chr13:39037779-39038482 | Common:2; Rare:193 | ||||
| chr13:40771122-40771338 | Common:3; Rare:72 | ||||
| chr13:41132726-41133053 | Common:1; Rare:86 | ||||
| chr13:41263480-41263881 | Common:1; Rare:91 | ||||
| chr13:41868454-41868665 | Common:1; Rare:43 | ||||
| chr13:41961050-41961296 | Common:3; Rare:80 | ||||
| chr13:42271779-42272046 | Common:2; Rare:76 | ||||
| chr13:42992189-42992376 | Common:3; Rare:37 | ||||
| chr13:42992382-42992439 | Rare:12 | ||||
| chr13:43879444-43879659 | Common:1; Rare:55 |