| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:111860472-111860619 | Rare:30 | ||||
| chr3:112092923-112093041 | Rare:20 | ||||
| chr3:119659139-119659265 | Common:1; Rare:35 | ||||
| chr3:119666077-119666331 | Common:4; Rare:48 | ||||
| chr3:120095037-120095245 | Rare:58 | ||||
| chr3:120448778-120448942 | Rare:28 | ||||
| chr3:120448950-120449005 | Rare:9 | ||||
| chr3:123284623-123284937 | Common:1; Rare:79; Clinvar:1 | ||||
| chr3:123335208-123335510 | Common:2; Rare:61 | ||||
| chr3:123386131-123386291 | Common:2; Rare:32 | ||||
| chr3:123447057-123447257 | Rare:49 | ||||
| chr3:123447410-123447587 | Common:1; Rare:66 | ||||
| chr3:123447941-123448240 | Common:1; Rare:92; Clinvar (pathogenic):1 | ||||
| chr3:123449081-123449226 | Rare:30 | ||||
| chr3:125990535-125990596 | Common:1; Rare:18 |