| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:40771300-40771333 | Common:1; Rare:8 | ||||
| chr13:40789385-40789640 | Common:2; Rare:88; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:41060157-41060511 | Common:3; Rare:120 | ||||
| chr13:41060836-41060927 | Common:6; Rare:57 | ||||
| chr13:41061035-41061645 | Common:4; Rare:205 | ||||
| chr13:41132776-41132980 | Rare:52 | ||||
| chr13:41263552-41263867 | Common:1; Rare:76 | ||||
| chr13:41457320-41457547 | Common:2; Rare:66 | ||||
| chr13:42040387-42040587 | Common:1; Rare:62 | ||||
| chr13:43879467-43879659 | Common:1; Rare:51 | ||||
| chr13:43879743-43879910 | Common:15; Rare:52 | ||||
| chr13:44576210-44576362 | Common:1; Rare:39 | ||||
| chr13:44577105-44577189 | Rare:19 | ||||
| chr13:44577289-44577645 | Common:3; Rare:127 | ||||
| chr13:44989428-44989592 | Rare:63 |