| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85678721-85679037 | Rare:106 | ||||
| chr6:129505058-129505322 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:169162898-169162942 | Rare:5 | ||||
| chr7:41705406-41705614 | Common:1; Rare:44 | ||||
| chr7:44986638-44986758 | Common:2; Rare:57 | ||||
| chr7:45768935-45769141 | Common:1; Rare:59 | ||||
| chr7:65750908-65751080 | Common:2; Rare:71 | ||||
| chr7:66493549-66493727 | Common:2; Rare:71 | ||||
| chr7:66592313-66592449 | Common:2; Rare:47 | ||||
| chr7:66654426-66654567 | Common:1; Rare:55 | ||||
| chr7:67302408-67302674 | Common:5; Rare:83 | ||||
| chr7:73005894-73006140 | Rare:20 | ||||
| chr7:74890556-74890820 | Common:2; Rare:78 | ||||
| chr7:94392168-94392319 | Common:1; Rare:20 | ||||
| chr7:94395563-94395882 | Common:3; Rare:63 |