| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51452428-51452542 | Rare:27 | ||||
| chr13:51452598-51452799 | Common:1; Rare:45 | ||||
| chr13:51452873-51453740 | Common:4; Rare:296 | ||||
| chr13:51454095-51454267 | Common:1; Rare:45 | ||||
| chr13:51583757-51584108 | Common:2; Rare:88 | ||||
| chr13:51584256-51584652 | Common:4; Rare:119 | ||||
| chr13:51584714-51585019 | Common:1; Rare:88 | ||||
| chr13:51803467-51803570 | Common:1; Rare:20 | ||||
| chr13:51803663-51803957 | Rare:80 | ||||
| chr13:51803979-51804407 | Common:2; Rare:125 | ||||
| chr13:52011854-52011984 | Common:1; Rare:45 | ||||
| chr13:52012050-52012487 | Common:2; Rare:163; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:52129001-52129128 | Common:1; Rare:28 | ||||
| chr13:52158925-52159119 | Common:3; Rare:36 | ||||
| chr13:52159160-52159324 | Common:3; Rare:29 |