| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118548071-118548362 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:118651497-118651791 | Common:4; Rare:99 | ||||
| chr6:118893741-118894309 | Common:10; Rare:159 | ||||
| chr6:118934950-118935095 | Common:4; Rare:48 | ||||
| chr6:119349727-119349930 | Common:2; Rare:72 | ||||
| chr6:121334448-121334589 | Common:4; Rare:58 | ||||
| chr6:121334699-121334801 | Common:1; Rare:19 | ||||
| chr6:122399318-122399708 | Common:6; Rare:141 | ||||
| chr6:122471706-122471950 | Common:4; Rare:89 | ||||
| chr6:122789083-122789415 | Common:2; Rare:91 | ||||
| chr6:122789610-122789812 | Common:1; Rare:41 | ||||
| chr6:124963023-124963308 | Common:1; Rare:94 | ||||
| chr6:125154228-125154478 | Common:2; Rare:67 | ||||
| chr6:125749366-125749694 | Common:6; Rare:133 | ||||
| chr6:125780864-125780952 | Rare:18 |