| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:38350215-38350408 | Rare:63 | ||||
| chr13:39038081-39038624 | Common:1; Rare:143 | ||||
| chr13:40771138-40771400 | Common:3; Rare:80 | ||||
| chr13:40789368-40789644 | Common:2; Rare:94; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:41060384-41060522 | Rare:53 | ||||
| chr13:41060840-41061043 | Common:16; Rare:124 | ||||
| chr13:41061140-41061586 | Common:4; Rare:149 | ||||
| chr13:41132720-41132980 | Rare:70 | ||||
| chr13:41194426-41194685 | Common:2; Rare:57 | ||||
| chr13:41960895-41961169 | Common:2; Rare:87 | ||||
| chr13:43879476-43879654 | Common:1; Rare:47 | ||||
| chr13:43879684-43879932 | Common:18; Rare:67 | ||||
| chr13:44989432-44989602 | Rare:66 | ||||
| chr13:45120358-45120582 | Common:2; Rare:69 | ||||
| chr13:45341036-45341624 | Common:4; Rare:264 |