| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52012110-52012428 | Common:2; Rare:104; Clinvar:1 | ||||
| chr13:52159553-52159724 | Common:1; Rare:29 | ||||
| chr13:52450592-52450685 | Rare:27 | ||||
| chr13:52455344-52455510 | Common:3; Rare:54 | ||||
| chr13:52652425-52652933 | Common:3; Rare:149 | ||||
| chr13:60397122-60397391 | Common:4; Rare:98 | ||||
| chr13:67230310-67230651 | Common:2; Rare:111 | ||||
| chr13:72727598-72727950 | Common:4; Rare:129 | ||||
| chr13:72781828-72782198 | Common:1; Rare:145 | ||||
| chr13:75549475-75549823 | Common:8; Rare:85 | ||||
| chr13:76991952-76992181 | Common:3; Rare:110; Clinvar:20; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr13:77027136-77027325 | Common:6; Rare:64 | ||||
| chr13:77918685-77918935 | Common:2; Rare:53 | ||||
| chr13:79405784-79405898 | Rare:40 | ||||
| chr13:79406219-79406320 | Common:2; Rare:29 |