| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:114056515-114056783 | Common:2; Rare:100 | ||||
| chr3:119498412-119498666 | Common:4; Rare:81 | ||||
| chr3:120093685-120093777 | Rare:27 | ||||
| chr3:120742503-120742843 | Common:2; Rare:91 | ||||
| chr3:121749637-121750032 | Common:1; Rare:91 | ||||
| chr3:121834964-121835238 | Common:3; Rare:87; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122416002-122416225 | Common:1; Rare:75 | ||||
| chr3:122564231-122564427 | Common:3; Rare:57 | ||||
| chr3:123961199-123961534 | Common:3; Rare:132 | ||||
| chr3:126083974-126084195 | Common:2; Rare:64 | ||||
| chr3:127598214-127598458 | Common:3; Rare:73 | ||||
| chr3:128052161-128052539 | Common:2; Rare:129 | ||||
| chr3:128067122-128067463 | Rare:73 | ||||
| chr3:128726103-128726356 | Common:3; Rare:78; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:128879417-128879663 | Common:4; Rare:116; Clinvar:2; Clinvar (benign):2 |