| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101217850-101218198 | Common:4; Rare:111 | ||||
| chr7:101252260-101252423 | Rare:36 | ||||
| chr7:101321729-101321860 | Common:2; Rare:47 | ||||
| chr7:102433328-102433635 | Common:2; Rare:79 | ||||
| chr7:102464844-102465022 | Common:1; Rare:71 | ||||
| chr7:102748696-102749026 | Common:2; Rare:76 | ||||
| chr7:103149290-103149380 | Common:2; Rare:22 | ||||
| chr7:104207973-104208112 | Common:2; Rare:59 | ||||
| chr7:105013562-105013719 | Common:1; Rare:50 | ||||
| chr7:105014108-105014268 | Common:1; Rare:64 | ||||
| chr7:105532082-105532242 | Common:1; Rare:41 | ||||
| chr7:105876477-105876818 | Common:6; Rare:100 | ||||
| chr7:106284911-106285262 | Common:2; Rare:132 | ||||
| chr7:106285539-106285563 | Rare:7 | ||||
| chr7:107563846-107564047 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):5 |