| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38875864-38876059 | Common:2; Rare:70 | ||||
| chr2:38960345-38960456 | Common:1; Rare:44 | ||||
| chr2:38960473-38960521 | Rare:20 | ||||
| chr2:39120167-39120223 | Rare:17 | ||||
| chr2:39120232-39120510 | Common:1; Rare:124; Clinvar:2; Clinvar (benign):10 | ||||
| chr2:39120939-39121252 | Common:3; Rare:124 | ||||
| chr2:39123741-39124012 | Rare:73 | ||||
| chr2:39124041-39124075 | Rare:10 | ||||
| chr2:39124160-39124591 | Common:1; Rare:140 | ||||
| chr2:39124779-39124888 | Rare:19 | ||||
| chr2:39436775-39437059 | Common:4; Rare:110 | ||||
| chr2:39437093-39437450 | Common:4; Rare:125 | ||||
| chr2:39778931-39779048 | Rare:34 | ||||
| chr2:39779136-39779396 | Common:4; Rare:92 | ||||
| chr2:42047528-42048071 | Common:6; Rare:167 |