| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36346269-36346530 | Common:3; Rare:71; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:37000742-37000805 | Rare:26 | ||||
| chr13:37059604-37059728 | Common:1; Rare:44 | ||||
| chr13:39037982-39038482 | Common:1; Rare:129 | ||||
| chr13:40666586-40666795 | Common:2; Rare:77 | ||||
| chr13:41061156-41061594 | Common:4; Rare:147 | ||||
| chr13:43879453-43879627 | Rare:47 | ||||
| chr13:44989456-44989601 | Rare:51 | ||||
| chr13:45341077-45341563 | Common:4; Rare:232 | ||||
| chr13:46052718-46052798 | Common:1; Rare:22 | ||||
| chr13:48303690-48303900 | Rare:64; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:49247836-49247982 | Rare:44 | ||||
| chr13:49443996-49444308 | Common:1; Rare:106 | ||||
| chr13:49585491-49585633 | Common:1; Rare:48 | ||||
| chr13:50081978-50082265 | Common:1; Rare:79 |