| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:127588292-127588501 | Rare:91 | ||||
| chr7:127651862-127652208 | Common:2; Rare:98 | ||||
| chr7:128476645-128476815 | Common:1; Rare:64 | ||||
| chr7:129054867-129055234 | Common:2; Rare:69 | ||||
| chr7:129611633-129611781 | Common:1; Rare:49 | ||||
| chr7:130205379-130205520 | Rare:64 | ||||
| chr7:131327711-131327894 | Rare:63 | ||||
| chr7:134646592-134646856 | Common:5; Rare:75 | ||||
| chr7:135170645-135170816 | Common:2; Rare:66 | ||||
| chr7:135662403-135662515 | Common:2; Rare:47 | ||||
| chr7:137343474-137343600 | Rare:52 | ||||
| chr7:139133691-139133828 | Rare:38 | ||||
| chr7:139359692-139359968 | Common:2; Rare:113 | ||||
| chr7:141014928-141015074 | Rare:34 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 |