| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105522207-105522339 | Common:1; Rare:50 | ||||
| chr7:105532055-105532225 | Common:2; Rare:46 | ||||
| chr7:106112234-106112445 | Common:3; Rare:60 | ||||
| chr7:106112478-106112634 | Rare:64 | ||||
| chr7:106284969-106285285 | Common:2; Rare:117 | ||||
| chr7:107091516-107091658 | Common:1; Rare:19 | ||||
| chr7:107168728-107169004 | Rare:93 | ||||
| chr7:107563861-107564022 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:107580123-107580286 | Common:2; Rare:63 | ||||
| chr7:107743582-107743801 | Common:3; Rare:83 | ||||
| chr7:107744058-107744176 | Rare:40 | ||||
| chr7:107891034-107891252 | Rare:101; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:108526071-108526475 | Common:5; Rare:123 | ||||
| chr7:108569576-108569958 | Common:1; Rare:140 | ||||
| chr7:111562473-111562672 | Rare:70 |