| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122384046-122384271 | Common:1; Rare:163 | ||||
| chr3:122416010-122416412 | Common:5; Rare:175 | ||||
| chr3:122496120-122497001 | Common:3; Rare:224 | ||||
| chr3:122514775-122515041 | Common:5; Rare:133 | ||||
| chr3:122564240-122564427 | Common:6; Rare:109 | ||||
| chr3:122564545-122564711 | Rare:53 | ||||
| chr3:122680560-122680874 | Rare:169 | ||||
| chr3:122793642-122793871 | Common:5; Rare:112 | ||||
| chr3:122794787-122795176 | Common:6; Rare:235 | ||||
| chr3:123066897-123067187 | Rare:125 | ||||
| chr3:123201720-123202033 | Common:3; Rare:169 | ||||
| chr3:123584957-123585345 | Common:4; Rare:212 | ||||
| chr3:123585484-123585658 | Rare:46 | ||||
| chr3:123961183-123961538 | Common:3; Rare:174 | ||||
| chr3:124730317-124730564 | Common:7; Rare:201; Clinvar:6; Clinvar (benign):7 |