| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75482392-75482550 | Common:3; Rare:41 | ||||
| chr13:75537777-75538114 | Common:3; Rare:107 | ||||
| chr13:75549378-75549847 | Common:9; Rare:126 | ||||
| chr13:75550064-75550145 | Common:1; Rare:23 | ||||
| chr13:75635772-75635890 | Common:1; Rare:30 | ||||
| chr13:75635993-75636366 | Common:2; Rare:94 | ||||
| chr13:76992001-76992203 | Common:3; Rare:91; Clinvar:15; Clinvar (benign):11; Clinvar (pathogenic):3 | ||||
| chr13:77027137-77027293 | Common:5; Rare:49 | ||||
| chr13:77327069-77327171 | Rare:47 | ||||
| chr13:77918689-77918942 | Common:2; Rare:55 | ||||
| chr13:77919397-77919528 | Rare:51; Clinvar:1 | ||||
| chr13:77919564-77919728 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:79405703-79405918 | Common:1; Rare:69 | ||||
| chr13:79406203-79406339 | Common:4; Rare:41 | ||||
| chr13:93226684-93226895 | Common:2; Rare:41; Clinvar (benign):1 |