| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:40666586-40666790 | Common:2; Rare:76 | ||||
| chr13:40771135-40771380 | Common:3; Rare:78 | ||||
| chr13:40789326-40789663 | Common:2; Rare:118; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:41060854-41061046 | Common:16; Rare:118 | ||||
| chr13:41061356-41061622 | Common:2; Rare:80 | ||||
| chr13:41132735-41132959 | Rare:59 | ||||
| chr13:41263519-41263611 | Rare:21 | ||||
| chr13:41311219-41311390 | Common:2; Rare:68 | ||||
| chr13:41373950-41374217 | Common:4; Rare:54 | ||||
| chr13:43786870-43787031 | Rare:52 | ||||
| chr13:43879459-43879614 | Rare:42 | ||||
| chr13:43879621-43879927 | Common:19; Rare:77 | ||||
| chr13:44435159-44435493 | Common:3; Rare:99 | ||||
| chr13:44436627-44436711 | Common:1; Rare:28 | ||||
| chr13:44989147-44989219 | Rare:31 |