| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75549363-75549850 | Common:9; Rare:129 | ||||
| chr13:75635714-75635957 | Common:1; Rare:74 | ||||
| chr13:75636033-75636506 | Common:2; Rare:105 | ||||
| chr13:75760418-75760726 | Common:2; Rare:67 | ||||
| chr13:76991975-76992270 | Common:3; Rare:135; Clinvar:21; Clinvar (benign):15; Clinvar (pathogenic):5 | ||||
| chr13:77026892-77026948 | Common:1; Rare:15 | ||||
| chr13:77026953-77027004 | Rare:17 | ||||
| chr13:77027120-77027293 | Common:5; Rare:57 | ||||
| chr13:77918536-77918932 | Common:2; Rare:93; Clinvar (benign):2 | ||||
| chr13:77919160-77919592 | Common:1; Rare:133; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:78659057-78659226 | Common:2; Rare:119 | ||||
| chr13:79405770-79405911 | Rare:51 | ||||
| chr13:79406195-79406339 | Common:4; Rare:44 | ||||
| chr13:79480996-79481484 | Common:2; Rare:188 | ||||
| chr13:80339236-80339454 | Common:3; Rare:59 |