| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:10973097-10973363 | Common:3; Rare:78 | ||||
| chr7:13806642-13806822 | Common:4; Rare:60 | ||||
| chr7:16347841-16348141 | Common:2; Rare:61 | ||||
| chr7:19194317-19194587 | Common:7; Rare:81 | ||||
| chr7:23471112-23471494 | Common:2; Rare:112 | ||||
| chr7:23474343-23474739 | Common:1; Rare:126 | ||||
| chr7:25855034-25855342 | Common:2; Rare:68 | ||||
| chr7:25856959-25857220 | Common:11; Rare:73 | ||||
| chr7:25951279-25951539 | Common:2; Rare:74 | ||||
| chr7:26193252-26193692 | Rare:155; Clinvar (benign):2 | ||||
| chr7:29684876-29685022 | Common:1; Rare:51 | ||||
| chr7:30642320-30642458 | Common:1; Rare:42 | ||||
| chr7:32728580-32728890 | Common:11; Rare:106 | ||||
| chr7:32942514-32942692 | Common:2; Rare:54 | ||||
| chr7:35185815-35185980 | Common:1; Rare:41 |