| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123620443-123620587 | Common:1; Rare:23 | ||||
| chr3:123692329-123692471 | Rare:32 | ||||
| chr3:123700912-123701341 | Common:1; Rare:87; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:124730317-124730474 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:125375132-125375431 | Rare:86 | ||||
| chr3:125520133-125520297 | Rare:57 | ||||
| chr3:125595214-125595426 | Common:2; Rare:63 | ||||
| chr3:125595498-125595672 | Common:1; Rare:59 | ||||
| chr3:126084103-126084219 | Common:1; Rare:51 | ||||
| chr3:126475922-126476247 | Common:6; Rare:74 | ||||
| chr3:127598190-127598458 | Common:3; Rare:78 | ||||
| chr3:127672808-127673077 | Common:4; Rare:127 | ||||
| chr3:127677272-127677507 | Common:1; Rare:68 | ||||
| chr3:127736001-127736299 | Common:2; Rare:43 | ||||
| chr3:127822333-127822747 | Common:1; Rare:96 |