| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105962989-105963312 | Common:2; Rare:51 | ||||
| chr7:106112477-106112644 | Common:1; Rare:70 | ||||
| chr7:106284096-106284141 | Rare:13 | ||||
| chr7:106284890-106285276 | Common:2; Rare:155 | ||||
| chr7:106285539-106285592 | Rare:14 | ||||
| chr7:106661152-106661275 | Common:1; Rare:17 | ||||
| chr7:107563861-107564028 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107580147-107580294 | Common:2; Rare:59 | ||||
| chr7:107743582-107743819 | Common:3; Rare:93 | ||||
| chr7:107744001-107744190 | Common:1; Rare:61 | ||||
| chr7:107891419-107891435 | Rare:1 | ||||
| chr7:108526099-108526455 | Common:5; Rare:111 | ||||
| chr7:108569576-108570019 | Common:2; Rare:158 | ||||
| chr7:111090840-111091133 | Rare:51 | ||||
| chr7:112206339-112206762 | Common:2; Rare:141 |