| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:94712543-94712693 | Common:1; Rare:33 | ||||
| chr13:95300802-95300993 | Common:1; Rare:33 | ||||
| chr13:95301267-95301550 | Common:1; Rare:90 | ||||
| chr13:95301762-95301823 | Common:1; Rare:10 | ||||
| chr13:95676831-95677161 | Common:2; Rare:127 | ||||
| chr13:96053149-96053175 | Rare:7 | ||||
| chr13:96053353-96053523 | Common:2; Rare:73 | ||||
| chr13:99200662-99200909 | Common:6; Rare:117 | ||||
| chr13:100088905-100089195 | Rare:113; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:100674751-100675060 | Common:3; Rare:126 | ||||
| chr13:102596782-102597188 | Common:2; Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:102798917-102799339 | Common:1; Rare:83 | ||||
| chr13:102845743-102846097 | Common:8; Rare:92; Clinvar:2; Clinvar (benign):4 | ||||
| chr13:102846142-102846347 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:106567577-106567777 | Rare:64 |