| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101363002-101363130 | Common:2; Rare:51 | ||||
| chr7:101815637-101816083 | Common:1; Rare:117 | ||||
| chr7:102464840-102464988 | Common:1; Rare:63 | ||||
| chr7:102748692-102749191 | Common:3; Rare:130 | ||||
| chr7:103074773-103074886 | Rare:48 | ||||
| chr7:103149055-103149372 | Common:4; Rare:90 | ||||
| chr7:104207973-104208077 | Common:1; Rare:45 | ||||
| chr7:105014052-105014268 | Common:3; Rare:87 | ||||
| chr7:105532086-105532256 | Common:1; Rare:43 | ||||
| chr7:105876470-105876858 | Common:7; Rare:113 | ||||
| chr7:106112200-106112485 | Common:3; Rare:92 | ||||
| chr7:106284885-106285437 | Common:6; Rare:208 | ||||
| chr7:106285539-106285616 | Rare:21 | ||||
| chr7:106661150-106661275 | Common:1; Rare:17 | ||||
| chr7:107563861-107564021 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):3 |