| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:116679538-116679848 | Common:2; Rare:57 | ||||
| chr7:116687965-116688228 | Common:1; Rare:40 | ||||
| chr7:116716353-116716412 | Rare:4 | ||||
| chr7:116748365-116748531 | Rare:26 | ||||
| chr7:116755063-116755416 | Common:1; Rare:66; Clinvar:4; Clinvar (benign):4 | ||||
| chr7:116757470-116757785 | Common:2; Rare:89; Clinvar:11; Clinvar (benign):7 | ||||
| chr7:116771976-116772049 | Rare:25 | ||||
| chr7:116794683-116794930 | Common:1; Rare:46 | ||||
| chr7:116972435-116972543 | Rare:20 | ||||
| chr7:116972785-116973084 | Rare:50 | ||||
| chr7:117263756-117263981 | Rare:29 | ||||
| chr7:121360041-121360259 | Rare:45 | ||||
| chr7:121365634-121365811 | Common:1; Rare:31 | ||||
| chr7:121983759-121983996 | Rare:49 | ||||
| chr7:122024202-122024243 | Rare:5 |