| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99408755-99409034 | Common:1; Rare:81 | ||||
| chr7:99438744-99439106 | Common:3; Rare:100 | ||||
| chr7:99472659-99472921 | Common:4; Rare:83 | ||||
| chr7:99500238-99500430 | Common:2; Rare:52 | ||||
| chr7:99552075-99552182 | Rare:39 | ||||
| chr7:99558335-99558739 | Common:2; Rare:126 | ||||
| chr7:100090410-100090655 | Common:2; Rare:72 | ||||
| chr7:100101341-100101745 | Common:1; Rare:155; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:100119301-100119728 | Rare:133 | ||||
| chr7:100428679-100428817 | Common:3; Rare:51 | ||||
| chr7:100429180-100429462 | Common:3; Rare:117 | ||||
| chr7:100603027-100603247 | Common:2; Rare:33 | ||||
| chr7:100852598-100852762 | Common:1; Rare:41 | ||||
| chr7:101217849-101218198 | Common:4; Rare:111 | ||||
| chr7:101244688-101244993 | Common:1; Rare:121 |