| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99408824-99409018 | Common:1; Rare:64 | ||||
| chr7:99438761-99438982 | Common:1; Rare:60 | ||||
| chr7:99500284-99500417 | Common:1; Rare:36 | ||||
| chr7:99558541-99558695 | Common:2; Rare:54 | ||||
| chr7:100088900-100089027 | Common:1; Rare:44 | ||||
| chr7:100101329-100101672 | Common:1; Rare:129 | ||||
| chr7:100119308-100119707 | Rare:119 | ||||
| chr7:100148716-100148984 | Common:1; Rare:110 | ||||
| chr7:100586123-100586315 | Common:2; Rare:64 | ||||
| chr7:101321707-101321849 | Common:2; Rare:51 | ||||
| chr7:103297327-103297456 | Common:1; Rare:39 | ||||
| chr7:105014091-105014214 | Common:1; Rare:53 | ||||
| chr7:105532061-105532225 | Rare:44 | ||||
| chr7:106285539-106285551 | Rare:5 | ||||
| chr7:107563879-107564014 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):3 |