| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:122471733-122471921 | Common:2; Rare:60 | ||||
| chr6:125781049-125781156 | Rare:19 | ||||
| chr6:125986335-125986548 | Common:1; Rare:72 | ||||
| chr6:127266785-127266899 | Common:1; Rare:42 | ||||
| chr6:127343337-127343429 | Rare:18 | ||||
| chr6:127343545-127343584 | Rare:13 | ||||
| chr6:128520569-128520757 | Rare:73 | ||||
| chr6:129490616-129490717 | Common:1; Rare:17 | ||||
| chr6:131628172-131628463 | Common:2; Rare:75 | ||||
| chr6:132401439-132401595 | Common:1; Rare:45 | ||||
| chr6:133889095-133889194 | Rare:16 | ||||
| chr6:133953038-133953241 | Common:2; Rare:61 | ||||
| chr6:134174850-134175130 | Common:1; Rare:124 | ||||
| chr6:135054792-135055013 | Common:5; Rare:63 | ||||
| chr6:135497618-135497901 | Common:4; Rare:103; Clinvar:1; Clinvar (benign):2 |