| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122416039-122416225 | Common:1; Rare:61 | ||||
| chr3:122564180-122564428 | Common:3; Rare:70 | ||||
| chr3:122795571-122795713 | Rare:29 | ||||
| chr3:123404410-123404663 | Rare:34 | ||||
| chr3:123416216-123416500 | Common:1; Rare:50 | ||||
| chr3:123585036-123585149 | Common:1; Rare:47 | ||||
| chr3:123585489-123585557 | Rare:12 | ||||
| chr3:123620205-123620597 | Common:1; Rare:88; Clinvar:5 | ||||
| chr3:123692335-123692468 | Rare:29 | ||||
| chr3:123698849-123698913 | Common:1; Rare:9 | ||||
| chr3:123700912-123701347 | Common:1; Rare:87; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:124730367-124730464 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:125357247-125357338 | Common:1; Rare:28 | ||||
| chr3:125375222-125375426 | Rare:60 | ||||
| chr3:125520158-125520271 | Rare:38 |