| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37598764-37598809 | Rare:5 | ||||
| chr13:37869759-37869892 | Common:1; Rare:31 | ||||
| chr13:38349540-38349920 | Common:4; Rare:129; Clinvar (pathogenic):1 | ||||
| chr13:38350249-38350365 | Rare:34 | ||||
| chr13:39038087-39038433 | Common:1; Rare:87 | ||||
| chr13:39603119-39603286 | Common:1; Rare:56 | ||||
| chr13:39655619-39655802 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771078-40771444 | Common:3; Rare:120 | ||||
| chr13:40789338-40789628 | Common:2; Rare:100; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41019247-41019421 | Rare:26 | ||||
| chr13:41060873-41060976 | Common:16; Rare:76 | ||||
| chr13:41061156-41061645 | Common:4; Rare:166 | ||||
| chr13:41132732-41133002 | Rare:72 | ||||
| chr13:41194489-41194659 | Common:2; Rare:41 | ||||
| chr13:41263488-41263611 | Rare:27 |