| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169751507-169751644 | Rare:49; Clinvar (benign):1 | ||||
| chr6:170306548-170306808 | Common:1; Rare:87 | ||||
| chr6:170554211-170554452 | Common:2; Rare:75 | ||||
| chr7:519120-519324 | Rare:52 | ||||
| chr7:727246-727308 | Rare:20; Clinvar:1 | ||||
| chr7:727629-727975 | Common:1; Rare:68 | ||||
| chr7:1028301-1028465 | Rare:63 | ||||
| chr7:1088007-1088188 | Common:1; Rare:54 | ||||
| chr7:1138198-1138383 | Common:1; Rare:61 | ||||
| chr7:1537256-1537490 | Rare:77 | ||||
| chr7:1570007-1570146 | Common:1; Rare:45 | ||||
| chr7:2242178-2242270 | Common:2; Rare:53 | ||||
| chr7:2314348-2314682 | Common:5; Rare:127 | ||||
| chr7:2354069-2354114 | Rare:20 | ||||
| chr7:2403282-2403622 | Common:1; Rare:133 |