| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169725308-169725452 | Rare:30 | ||||
| chr6:169725474-169725545 | Common:1; Rare:22 | ||||
| chr6:169751471-169751833 | Common:2; Rare:138; Clinvar (benign):5 | ||||
| chr6:170306548-170306824 | Common:3; Rare:90 | ||||
| chr6:170553196-170553370 | Common:3; Rare:76 | ||||
| chr6:170554200-170554624 | Common:3; Rare:124 | ||||
| chr7:691788-691932 | Common:1; Rare:40 | ||||
| chr7:727241-727314 | Rare:24; Clinvar:1 | ||||
| chr7:727613-727897 | Common:1; Rare:50 | ||||
| chr7:830811-830979 | Common:2; Rare:42 | ||||
| chr7:975481-975650 | Common:1; Rare:82 | ||||
| chr7:1028278-1028522 | Common:1; Rare:94 | ||||
| chr7:1055129-1055372 | Common:1; Rare:82 | ||||
| chr7:1138196-1138466 | Common:2; Rare:83 | ||||
| chr7:1448372-1448622 | Rare:71 |