| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:74134279-74134535 | Common:3; Rare:92 | ||||
| chr13:75482133-75482265 | Common:1; Rare:28 | ||||
| chr13:75549409-75549831 | Common:8; Rare:112 | ||||
| chr13:75760331-75760971 | Common:2; Rare:176 | ||||
| chr13:76886406-76886673 | Common:2; Rare:82 | ||||
| chr13:76992038-76992270 | Common:1; Rare:107; Clinvar:13; Clinvar (benign):11; Clinvar (pathogenic):5 | ||||
| chr13:77027118-77027287 | Common:5; Rare:56 | ||||
| chr13:77327036-77327380 | Common:1; Rare:127 | ||||
| chr13:77697448-77697697 | Common:1; Rare:68 | ||||
| chr13:77918532-77918883 | Common:1; Rare:80; Clinvar (benign):2 | ||||
| chr13:77919397-77919497 | Rare:40; Clinvar:1 | ||||
| chr13:78659102-78659235 | Common:2; Rare:96 | ||||
| chr13:79405674-79405911 | Common:1; Rare:74 | ||||
| chr13:79406203-79406339 | Common:4; Rare:41 | ||||
| chr13:80339300-80339466 | Common:2; Rare:45 |