| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52455301-52455528 | Common:3; Rare:76 | ||||
| chr13:52652380-52652939 | Common:3; Rare:165 | ||||
| chr13:60163816-60164078 | Common:2; Rare:62 | ||||
| chr13:60397162-60397354 | Common:4; Rare:72 | ||||
| chr13:67230303-67230634 | Common:2; Rare:108 | ||||
| chr13:72727536-72727972 | Common:7; Rare:172 | ||||
| chr13:72781852-72782269 | Common:1; Rare:149 | ||||
| chr13:74134285-74134527 | Common:3; Rare:90 | ||||
| chr13:75549437-75549831 | Common:8; Rare:103 | ||||
| chr13:76991900-76992206 | Common:4; Rare:134; Clinvar:22; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr13:77027136-77027289 | Common:5; Rare:48 | ||||
| chr13:77918574-77918908 | Common:2; Rare:76; Clinvar (benign):2 | ||||
| chr13:78659121-78659235 | Common:2; Rare:83 | ||||
| chr13:79405703-79405902 | Common:1; Rare:62 | ||||
| chr13:79406219-79406339 | Common:3; Rare:38 |