| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123585489-123585590 | Rare:20 | ||||
| chr3:123692324-123692463 | Rare:31 | ||||
| chr3:123700963-123701343 | Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:124730362-124730468 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:124887386-124887515 | Rare:43 | ||||
| chr3:125375234-125375426 | Rare:57 | ||||
| chr3:125520111-125520315 | Rare:74 | ||||
| chr3:125595225-125595367 | Common:2; Rare:46 | ||||
| chr3:125595373-125595582 | Common:1; Rare:60 | ||||
| chr3:126084022-126084212 | Common:2; Rare:70 | ||||
| chr3:126179914-126180087 | Common:1; Rare:46 | ||||
| chr3:126180510-126180636 | Rare:19 | ||||
| chr3:126180800-126180828 | Rare:3 | ||||
| chr3:127598212-127598428 | Common:3; Rare:56 | ||||
| chr3:127628957-127629211 | Common:1; Rare:83 |