| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:50081937-50082307 | Common:1; Rare:105 | ||||
| chr13:50082654-50082823 | Common:1; Rare:42 | ||||
| chr13:50909601-50910420 | Common:3; Rare:201; Clinvar:7; Clinvar (benign):1 | ||||
| chr13:51451142-51451267 | Rare:19 | ||||
| chr13:51451483-51451647 | Rare:50 | ||||
| chr13:51452893-51453521 | Common:1; Rare:227 | ||||
| chr13:51453543-51453842 | Common:4; Rare:78 | ||||
| chr13:51583907-51584064 | Common:2; Rare:49 | ||||
| chr13:51584194-51584581 | Common:4; Rare:129 | ||||
| chr13:51584925-51584976 | Rare:11 | ||||
| chr13:51803271-51803568 | Common:2; Rare:48 | ||||
| chr13:51803677-51803909 | Rare:66 | ||||
| chr13:51804053-51804374 | Common:2; Rare:86 | ||||
| chr13:52012072-52012487 | Common:2; Rare:154; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:52158874-52159036 | Common:2; Rare:38 |