| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36919418-36919425 | Rare:1 | ||||
| chr13:37007908-37008176 | Common:1; Rare:67 | ||||
| chr13:37090965-37091122 | Common:2; Rare:34 | ||||
| chr13:37596577-37597017 | Common:2; Rare:73 | ||||
| chr13:40599920-40600267 | Common:4; Rare:64 | ||||
| chr13:40665739-40666063 | Common:1; Rare:95 | ||||
| chr13:42271401-42271547 | Common:2; Rare:42 | ||||
| chr13:42308365-42308536 | Common:1; Rare:43 | ||||
| chr13:44917980-44918104 | Common:3; Rare:79 | ||||
| chr13:45378288-45378511 | Common:2; Rare:62 | ||||
| chr13:46721573-46721732 | Common:1; Rare:20 | ||||
| chr13:46782673-46783013 | Common:1; Rare:73 | ||||
| chr13:48376678-48376968 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:48413063-48413402 | Rare:48 | ||||
| chr13:48975244-48975342 | Rare:20 |