| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49936079-49936123 | Rare:19 | ||||
| chr13:49936127-49936628 | Common:3; Rare:157 | ||||
| chr13:49936944-49937018 | Rare:14 | ||||
| chr13:49996282-49996384 | Common:2; Rare:24 | ||||
| chr13:49996605-49997145 | Common:4; Rare:143 | ||||
| chr13:49997213-49997544 | Rare:103 | ||||
| chr13:50081581-50081706 | Rare:26 | ||||
| chr13:50081781-50082350 | Common:2; Rare:152 | ||||
| chr13:50082496-50082822 | Common:1; Rare:82 | ||||
| chr13:50909602-50910446 | Common:3; Rare:208; Clinvar:7; Clinvar (benign):1 | ||||
| chr13:51222264-51222432 | Common:2; Rare:61 | ||||
| chr13:51451261-51451316 | Rare:9 | ||||
| chr13:51451516-51451716 | Rare:57 | ||||
| chr13:51451799-51452099 | Common:1; Rare:101 | ||||
| chr13:51452124-51452318 | Common:3; Rare:49 |