| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:71867242-71867481 | Common:1; Rare:56 | ||||
| chr13:72727576-72727972 | Common:7; Rare:151 | ||||
| chr13:72781728-72782194 | Common:1; Rare:178 | ||||
| chr13:74134258-74134600 | Common:4; Rare:129 | ||||
| chr13:75326318-75326652 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr13:75537784-75538144 | Common:3; Rare:114 | ||||
| chr13:75549426-75549821 | Common:8; Rare:101 | ||||
| chr13:75636033-75636347 | Common:2; Rare:70 | ||||
| chr13:76991975-76992213 | Common:3; Rare:109; Clinvar:18; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr13:77027136-77027274 | Common:5; Rare:46 | ||||
| chr13:77327048-77327259 | Common:1; Rare:85 | ||||
| chr13:77918536-77918942 | Common:2; Rare:95; Clinvar (benign):2 | ||||
| chr13:79405695-79405911 | Common:1; Rare:67 | ||||
| chr13:79406202-79406339 | Common:4; Rare:42 | ||||
| chr13:79481059-79481484 | Common:2; Rare:172 |