| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:132537683-132537858 | Common:1; Rare:57 | ||||
| chr10:132785889-132786414 | Common:1; Rare:276 | ||||
| chr10:132942509-132942679 | Common:2; Rare:50 | ||||
| chr10:133160338-133160524 | Common:2; Rare:70 | ||||
| chr10:133308810-133308926 | Rare:50 | ||||
| chr10:133373318-133373532 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr10:133378937-133379312 | Common:20; Rare:81 | ||||
| chr10:133393972-133394246 | Common:2; Rare:122 | ||||
| chr11:207327-207730 | Common:8; Rare:137 | ||||
| chr11:208615-208812 | Rare:60 | ||||
| chr11:209073-209473 | Common:1; Rare:146 | ||||
| chr11:236285-236560 | Common:9; Rare:99 | ||||
| chr11:236883-237026 | Rare:50 | ||||
| chr11:288910-289380 | Common:1; Rare:104 | ||||
| chr11:307997-308168 | Common:9; Rare:31 |