| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:117907065-117907280 | Common:4; Rare:97 | ||||
| chr6:118574043-118574511 | Common:2; Rare:105 | ||||
| chr6:118651559-118651730 | Common:3; Rare:54 | ||||
| chr6:118893874-118894287 | Common:4; Rare:123 | ||||
| chr6:118934454-118934605 | Rare:51 | ||||
| chr6:119078645-119078844 | Rare:70 | ||||
| chr6:119349736-119349920 | Common:2; Rare:61 | ||||
| chr6:121334431-121334586 | Common:4; Rare:67 | ||||
| chr6:121334699-121334804 | Common:1; Rare:20 | ||||
| chr6:121435520-121435831 | Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:122471701-122471937 | Common:3; Rare:81 | ||||
| chr6:122779403-122779747 | Rare:64 | ||||
| chr6:122788928-122789313 | Common:1; Rare:71 | ||||
| chr6:122789637-122789791 | Common:1; Rare:32 | ||||
| chr6:124963278-124963421 | Common:1; Rare:39 |