| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:125520162-125520319 | Rare:44 | ||||
| chr3:125595262-125595403 | Common:2; Rare:42 | ||||
| chr3:126084103-126084241 | Common:1; Rare:63 | ||||
| chr3:127598219-127598458 | Common:3; Rare:71 | ||||
| chr3:127628954-127629211 | Common:1; Rare:85 | ||||
| chr3:127672830-127673008 | Common:1; Rare:87 | ||||
| chr3:127823183-127823340 | Common:3; Rare:31 | ||||
| chr3:128052170-128052520 | Common:2; Rare:118 | ||||
| chr3:128123742-128124037 | Rare:84 | ||||
| chr3:128153368-128153496 | Rare:36 | ||||
| chr3:128487892-128488064 | Common:1; Rare:45 | ||||
| chr3:128488529-128488640 | Common:1; Rare:26 | ||||
| chr3:128493195-128493415 | Rare:73 | ||||
| chr3:128879425-128879675 | Common:4; Rare:123; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129160991-129161152 | Common:1; Rare:63 |