| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101217851-101218201 | Common:4; Rare:112 | ||||
| chr7:101244988-101245126 | Common:1; Rare:64 | ||||
| chr7:101252273-101252534 | Common:1; Rare:56 | ||||
| chr7:102464846-102465040 | Common:1; Rare:80 | ||||
| chr7:102748742-102749048 | Common:2; Rare:77 | ||||
| chr7:103074787-103075183 | Common:7; Rare:157 | ||||
| chr7:103149277-103149356 | Common:2; Rare:18 | ||||
| chr7:103344587-103344869 | Common:1; Rare:100 | ||||
| chr7:105014084-105014514 | Common:2; Rare:140 | ||||
| chr7:105532082-105532225 | Rare:39 | ||||
| chr7:105876467-105876822 | Common:6; Rare:104 | ||||
| chr7:106284841-106285215 | Common:2; Rare:142 | ||||
| chr7:106660961-106661052 | Rare:40 | ||||
| chr7:107563861-107564028 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107579908-107580305 | Common:4; Rare:127 |