| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37000157-37000404 | Common:2; Rare:52 | ||||
| chr13:37000508-37000815 | Common:3; Rare:97; Clinvar (pathogenic):1 | ||||
| chr13:37059600-37059751 | Common:1; Rare:51 | ||||
| chr13:38349552-38349917 | Common:3; Rare:124; Clinvar (pathogenic):1 | ||||
| chr13:38350215-38350289 | Rare:37 | ||||
| chr13:39038094-39038505 | Common:1; Rare:100 | ||||
| chr13:39603108-39603272 | Common:1; Rare:58 | ||||
| chr13:39655582-39655802 | Common:4; Rare:111; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771130-40771344 | Common:3; Rare:71 | ||||
| chr13:40789352-40789609 | Common:2; Rare:86; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:40982858-40982993 | Common:3; Rare:18 | ||||
| chr13:41019260-41019393 | Rare:20 | ||||
| chr13:41060406-41060557 | Rare:59 | ||||
| chr13:41060846-41061068 | Common:16; Rare:131 | ||||
| chr13:41061126-41061319 | Common:1; Rare:69 |