| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:104207966-104208197 | Common:5; Rare:103 | ||||
| chr7:105013576-105013743 | Common:1; Rare:55 | ||||
| chr7:105014002-105014288 | Common:3; Rare:108 | ||||
| chr7:105014360-105014492 | Rare:37 | ||||
| chr7:105532067-105532260 | Common:1; Rare:50 | ||||
| chr7:105679081-105679274 | Common:1; Rare:43 | ||||
| chr7:106284972-106285262 | Common:2; Rare:107 | ||||
| chr7:106660994-106661308 | Common:2; Rare:80 | ||||
| chr7:107563881-107564026 | Common:2; Rare:86; Clinvar (benign):4 | ||||
| chr7:107580147-107580304 | Common:2; Rare:61 | ||||
| chr7:107743604-107743868 | Common:5; Rare:101 | ||||
| chr7:107744032-107744254 | Rare:77 | ||||
| chr7:108526039-108526372 | Common:2; Rare:102 | ||||
| chr7:108569583-108569992 | Common:2; Rare:149 | ||||
| chr7:111562473-111562586 | Rare:53 |