| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39655559-39655781 | Common:4; Rare:113; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:40666432-40666645 | Common:1; Rare:78 | ||||
| chr13:40771071-40771523 | Common:3; Rare:139 | ||||
| chr13:40789278-40789672 | Common:3; Rare:132; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:40982883-40983035 | Common:3; Rare:25 | ||||
| chr13:41019325-41019351 | Rare:3 | ||||
| chr13:41019731-41019822 | Rare:11 | ||||
| chr13:41060059-41060590 | Common:3; Rare:189 | ||||
| chr13:41060809-41060847 | Common:1; Rare:26 | ||||
| chr13:41060862-41061053 | Common:16; Rare:113 | ||||
| chr13:41061340-41061595 | Common:2; Rare:75 | ||||
| chr13:41061622-41061838 | Common:1; Rare:84 | ||||
| chr13:41132496-41132551 | Rare:19 | ||||
| chr13:41132696-41133023 | Common:1; Rare:81 | ||||
| chr13:41194319-41194750 | Common:2; Rare:95 |