| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:72727560-72727988 | Common:19; Rare:480 | ||||
| chr13:72781818-72782219 | Common:3; Rare:417 | ||||
| chr13:73058743-73059182 | Common:2; Rare:304 | ||||
| chr13:74133653-74134633 | Common:15; Rare:447 | ||||
| chr13:75481940-75482221 | Common:2; Rare:59 | ||||
| chr13:75482289-75482860 | Common:10; Rare:168 | ||||
| chr13:75537757-75538220 | Common:11; Rare:371 | ||||
| chr13:75549426-75549890 | Common:15; Rare:212 | ||||
| chr13:75635766-75635884 | Common:1; Rare:30 | ||||
| chr13:75636168-75636382 | Common:1; Rare:102 | ||||
| chr13:75760463-75760756 | Common:2; Rare:68 | ||||
| chr13:76886251-76886711 | Common:8; Rare:325 | ||||
| chr13:76991874-76992268 | Common:12; Rare:430; Clinvar:70; Clinvar (benign):54; Clinvar (pathogenic):11 | ||||
| chr13:77027035-77027352 | Common:17; Rare:269 | ||||
| chr13:77326168-77326990 | Common:3; Rare:317 |