| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56051452-56051802 | Common:1; Rare:120; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:73683378-73683622 | Common:5; Rare:102 | ||||
| chr7:76047985-76048081 | Rare:22 | ||||
| chr7:87345515-87345709 | Common:3; Rare:61 | ||||
| chr7:90346553-90346709 | Common:2; Rare:61 | ||||
| chr7:91880682-91880771 | Common:1; Rare:25 | ||||
| chr7:92528484-92528807 | Common:3; Rare:95; Clinvar (benign):2 | ||||
| chr7:99325769-99325963 | Common:1; Rare:79 | ||||
| chr7:99408555-99408650 | Common:2; Rare:29 | ||||
| chr7:99408830-99408979 | Common:1; Rare:49 | ||||
| chr7:99558526-99558620 | Rare:32 | ||||
| chr7:100119352-100119657 | Rare:86 | ||||
| chr7:105013595-105013719 | Common:1; Rare:41 | ||||
| chr7:106284969-106285262 | Common:2; Rare:108 | ||||
| chr7:107563901-107563983 | Common:1; Rare:48; Clinvar (benign):1 |