| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123701436-123701597 | Common:1; Rare:51; Clinvar:7 | ||||
| chr3:124730367-124730474 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:125375237-125375426 | Rare:57 | ||||
| chr3:125520153-125520271 | Rare:41 | ||||
| chr3:125595258-125595345 | Common:2; Rare:33 | ||||
| chr3:126084098-126084212 | Common:1; Rare:45 | ||||
| chr3:126180510-126180861 | Common:1; Rare:76 | ||||
| chr3:126394805-126394953 | Common:1; Rare:42 | ||||
| chr3:126703958-126704284 | Common:4; Rare:90 | ||||
| chr3:127598235-127598446 | Common:3; Rare:53 | ||||
| chr3:127628970-127629251 | Common:1; Rare:92 | ||||
| chr3:128052173-128052515 | Common:2; Rare:117 | ||||
| chr3:128123760-128123979 | Rare:59 | ||||
| chr3:128153365-128153493 | Rare:35 | ||||
| chr3:128487788-128488059 | Common:2; Rare:69 |