| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120349304-120349594 | Common:2; Rare:89 | ||||
| chr3:120451028-120451329 | Rare:91 | ||||
| chr3:120596174-120596488 | Common:1; Rare:124 | ||||
| chr3:120742233-120742279 | Rare:13 | ||||
| chr3:120742503-120742782 | Common:2; Rare:78 | ||||
| chr3:120907875-120908291 | Rare:103 | ||||
| chr3:121545915-121546089 | Common:1; Rare:50 | ||||
| chr3:121749631-121750031 | Common:1; Rare:92 | ||||
| chr3:121834956-121835251 | Common:3; Rare:101; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383171-122383363 | Common:2; Rare:57 | ||||
| chr3:122384020-122384275 | Common:2; Rare:89 | ||||
| chr3:122416039-122416271 | Common:1; Rare:76 | ||||
| chr3:122514834-122515029 | Common:2; Rare:56 | ||||
| chr3:122793685-122793889 | Common:3; Rare:63 | ||||
| chr3:122794928-122795060 | Rare:46 |