| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:26222219-26222397 | Common:5; Rare:84 | ||||
| chr13:26253689-26254350 | Common:2; Rare:259 | ||||
| chr13:26557449-26557781 | Common:4; Rare:134 | ||||
| chr13:27171757-27172008 | Common:1; Rare:138 | ||||
| chr13:27251225-27251632 | Common:16; Rare:253 | ||||
| chr13:27251658-27252058 | Common:6; Rare:169 | ||||
| chr13:27270582-27270830 | Common:1; Rare:79 | ||||
| chr13:27424499-27424776 | Common:8; Rare:154 | ||||
| chr13:27449820-27450320 | Common:6; Rare:220 | ||||
| chr13:27450530-27450688 | Common:4; Rare:107 | ||||
| chr13:27620488-27620859 | Common:6; Rare:230 | ||||
| chr13:28138092-28138590 | Common:6; Rare:260 | ||||
| chr13:28139057-28139540 | Common:2; Rare:183 | ||||
| chr13:28659051-28659184 | Rare:104; Clinvar (pathogenic):2 | ||||
| chr13:29595407-29595842 | Common:6; Rare:249 |