| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:29195215-29195247 | Rare:12 | ||||
| chr7:29479976-29480036 | Common:2; Rare:14 | ||||
| chr7:29480041-29480175 | Rare:32 | ||||
| chr7:29563652-29563960 | Common:2; Rare:74 | ||||
| chr7:29565344-29565593 | Common:2; Rare:53 | ||||
| chr7:30478681-30478796 | Common:1; Rare:44 | ||||
| chr7:30504747-30504880 | Rare:56 | ||||
| chr7:30594345-30594432 | Common:1; Rare:21 | ||||
| chr7:30594728-30594949 | Common:3; Rare:103; Clinvar:5; Clinvar (benign):6 | ||||
| chr7:32495238-32495659 | Common:1; Rare:116 | ||||
| chr7:33062714-33062906 | Common:3; Rare:84 | ||||
| chr7:33129212-33129578 | Common:5; Rare:107 | ||||
| chr7:35694823-35695271 | Common:4; Rare:126 | ||||
| chr7:35800866-35801252 | Common:2; Rare:157 | ||||
| chr7:39566342-39566458 | Common:1; Rare:54 |