| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51804834-51804895 | Rare:11 | ||||
| chr13:51845158-51845328 | Rare:38 | ||||
| chr13:51958319-51958456 | Rare:50; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):9 | ||||
| chr13:51981455-51981616 | Rare:28 | ||||
| chr13:51998183-51998300 | Rare:22 | ||||
| chr13:51998811-51998893 | Rare:13 | ||||
| chr13:51999214-51999338 | Common:2; Rare:16 | ||||
| chr13:51999351-51999409 | Rare:7 | ||||
| chr13:52194267-52194631 | Common:2; Rare:87 | ||||
| chr13:52194636-52194677 | Rare:6 | ||||
| chr13:52599671-52599750 | Rare:21 | ||||
| chr13:52600090-52600216 | Rare:27 | ||||
| chr13:52600299-52600536 | Common:4; Rare:76 | ||||
| chr13:52600563-52600584 | Rare:4 | ||||
| chr13:52616874-52617110 | Common:2; Rare:55 |