| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32586227-32586582 | Common:2; Rare:107 | ||||
| chr13:33285703-33285968 | Common:1; Rare:59 | ||||
| chr13:33818004-33818222 | Common:1; Rare:98 | ||||
| chr13:34942163-34942294 | Common:3; Rare:39 | ||||
| chr13:35855541-35855705 | Common:1; Rare:35 | ||||
| chr13:35855713-35855732 | Rare:2 | ||||
| chr13:36297760-36297922 | Common:1; Rare:61 | ||||
| chr13:36345519-36345663 | Common:1; Rare:31 | ||||
| chr13:36346301-36346457 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346632-36346824 | Common:4; Rare:57 | ||||
| chr13:36999274-36999465 | Rare:76 | ||||
| chr13:37000246-37000404 | Common:2; Rare:30 | ||||
| chr13:37000725-37000835 | Rare:45; Clinvar (pathogenic):1 | ||||
| chr13:37001385-37001478 | Common:2; Rare:23 | ||||
| chr13:37059596-37059736 | Common:1; Rare:48 |