| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44276091-44276360 | Rare:66 | ||||
| chr7:44882755-44883155 | Common:1; Rare:139 | ||||
| chr7:44954870-44955330 | Common:2; Rare:77 | ||||
| chr7:44970849-44971249 | Common:1; Rare:125 | ||||
| chr7:44972211-44972355 | Common:1; Rare:38 | ||||
| chr7:44986600-44986811 | Common:3; Rare:99 | ||||
| chr7:45073444-45073844 | Common:12; Rare:172; Clinvar (benign):7 | ||||
| chr7:45768895-45769185 | Common:5; Rare:89 | ||||
| chr7:45978160-45978663 | Common:9; Rare:191 | ||||
| chr7:46088384-46088784 | Common:16; Rare:122 | ||||
| chr7:47045677-47045812 | Common:4; Rare:50 | ||||
| chr7:47202410-47202916 | Common:6; Rare:189 | ||||
| chr7:47254351-47254851 | Common:10; Rare:171 | ||||
| chr7:47326769-47327169 | Common:4; Rare:101 | ||||
| chr7:47327447-47327726 | Common:1; Rare:43 |