| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37059442-37059765 | Common:1; Rare:95 | ||||
| chr13:37869759-37869926 | Common:1; Rare:38 | ||||
| chr13:38349541-38349921 | Common:4; Rare:130; Clinvar (pathogenic):1 | ||||
| chr13:38350215-38350298 | Rare:39 | ||||
| chr13:39038087-39038488 | Common:1; Rare:98 | ||||
| chr13:39603099-39603435 | Common:2; Rare:122 | ||||
| chr13:39655619-39655735 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr13:39655741-39655879 | Common:2; Rare:51; Clinvar (benign):5 | ||||
| chr13:40771067-40771346 | Common:3; Rare:101 | ||||
| chr13:41061387-41061649 | Common:2; Rare:78 | ||||
| chr13:41132281-41132502 | Common:2; Rare:64 | ||||
| chr13:41132712-41132959 | Rare:64 | ||||
| chr13:41194460-41194659 | Common:2; Rare:48 | ||||
| chr13:41311026-41311309 | Common:1; Rare:100 | ||||
| chr13:41457289-41457547 | Common:2; Rare:76 |