| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119498812-119498886 | Rare:28 | ||||
| chr3:119579601-119579771 | Common:2; Rare:34 | ||||
| chr3:120094424-120094790 | Common:4; Rare:116 | ||||
| chr3:120349296-120349449 | Common:2; Rare:52 | ||||
| chr3:120595977-120596362 | Common:5; Rare:113 | ||||
| chr3:120742503-120742772 | Common:2; Rare:76 | ||||
| chr3:121749633-121750021 | Common:1; Rare:89 | ||||
| chr3:121834987-121835263 | Common:3; Rare:95; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383332 | Common:1; Rare:43 | ||||
| chr3:122384068-122384292 | Common:3; Rare:81 | ||||
| chr3:122416031-122416241 | Common:1; Rare:70 | ||||
| chr3:122514873-122515006 | Common:1; Rare:38 | ||||
| chr3:122564236-122564437 | Common:3; Rare:59 | ||||
| chr3:123585489-123585599 | Rare:21 | ||||
| chr3:123692353-123692464 | Rare:23 |