| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:74133742-74133857 | Common:3; Rare:22 | ||||
| chr13:74134264-74134525 | Common:3; Rare:98 | ||||
| chr13:75549439-75549837 | Common:8; Rare:104 | ||||
| chr13:75635782-75635853 | Common:1; Rare:17 | ||||
| chr13:75636002-75636366 | Common:2; Rare:89 | ||||
| chr13:75760432-75761063 | Common:3; Rare:180 | ||||
| chr13:75788752-75788935 | Common:1; Rare:22 | ||||
| chr13:75804285-75804844 | Common:3; Rare:130 | ||||
| chr13:76886404-76886690 | Common:2; Rare:84 | ||||
| chr13:76992041-76992215 | Common:1; Rare:81; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr13:77027130-77027274 | Common:5; Rare:48 | ||||
| chr13:77326600-77326831 | Common:1; Rare:68 | ||||
| chr13:77697445-77697727 | Common:1; Rare:79 | ||||
| chr13:77918491-77918949 | Common:2; Rare:106; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:77919397-77919726 | Common:1; Rare:115; Clinvar:2; Clinvar (benign):1 |