| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30617216-30617863 | Common:1; Rare:201 | ||||
| chr13:30617872-30618046 | Rare:45 | ||||
| chr13:30932539-30932672 | Rare:27 | ||||
| chr13:30932679-30932714 | Rare:11 | ||||
| chr13:31162316-31162454 | Common:1; Rare:40 | ||||
| chr13:32031244-32031352 | Common:1; Rare:33 | ||||
| chr13:32031701-32031810 | Common:1; Rare:39 | ||||
| chr13:32315400-32315552 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32586248-32586593 | Common:2; Rare:107 | ||||
| chr13:33206022-33206025 | |||||
| chr13:33818013-33818197 | Common:1; Rare:79 | ||||
| chr13:34942156-34942318 | Common:3; Rare:47 | ||||
| chr13:35476682-35476820 | Common:1; Rare:22 | ||||
| chr13:35855511-35855751 | Common:1; Rare:59 | ||||
| chr13:36131161-36131227 | Rare:17 |