| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170584439-170584764 | Common:2; Rare:110 | ||||
| chr7:518300-518447 | Rare:39 | ||||
| chr7:519099-519289 | Rare:46 | ||||
| chr7:727236-727308 | Rare:23; Clinvar:1 | ||||
| chr7:1028268-1028526 | Common:2; Rare:99 | ||||
| chr7:1448372-1448622 | Rare:71 | ||||
| chr7:1570012-1570142 | Common:1; Rare:41 | ||||
| chr7:2242168-2242270 | Common:2; Rare:61 | ||||
| chr7:2354047-2354127 | Rare:41 | ||||
| chr7:2403282-2403637 | Common:1; Rare:139 | ||||
| chr7:2555493-2555850 | Common:5; Rare:98 | ||||
| chr7:4775510-4775718 | Common:4; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:5513732-5513886 | Common:1; Rare:65 | ||||
| chr7:5529742-5530081 | Common:1; Rare:161 | ||||
| chr7:5592703-5592839 | Common:1; Rare:46 |