| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:7969891-7970122 | Rare:34 | ||||
| chr7:17940476-17940563 | Common:1; Rare:35 | ||||
| chr7:19708997-19709206 | Common:4; Rare:73 | ||||
| chr7:20217388-20217603 | Common:1; Rare:49 | ||||
| chr7:21945788-21945936 | Common:3; Rare:65 | ||||
| chr7:22725700-22725870 | Common:2; Rare:45 | ||||
| chr7:22725991-22726256 | Rare:50 | ||||
| chr7:22726986-22727240 | Common:2; Rare:34 | ||||
| chr7:22822719-22822956 | Common:3; Rare:89 | ||||
| chr7:23105682-23105839 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181806-23181874 | Common:2; Rare:20 | ||||
| chr7:23181914-23182146 | Rare:101 | ||||
| chr7:23299160-23299356 | Common:3; Rare:85 | ||||
| chr7:23531769-23532083 | Common:2; Rare:122 | ||||
| chr7:24719107-24719407 | Common:5; Rare:72; Clinvar:2; Clinvar (benign):5 |