| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:90474732-90474968 | Common:2; Rare:96 | ||||
| chr5:90529521-90529820 | Common:1; Rare:116 | ||||
| chr5:90558540-90558824 | Common:5; Rare:77; Clinvar (benign):1 | ||||
| chr5:91380054-91380365 | Common:3; Rare:87 | ||||
| chr5:91383286-91383491 | Common:2; Rare:68 | ||||
| chr5:94111476-94111738 | Common:2; Rare:93 | ||||
| chr5:94618591-94618718 | Rare:35 | ||||
| chr5:95554957-95555183 | Rare:60 | ||||
| chr5:95646692-95646788 | Common:4; Rare:38 | ||||
| chr5:95731226-95731551 | Rare:97 | ||||
| chr5:95731775-95731869 | Rare:40 | ||||
| chr5:96702671-96702876 | Common:1; Rare:62 | ||||
| chr5:96876435-96876508 | Rare:14 | ||||
| chr5:96935807-96936145 | Common:10; Rare:113 | ||||
| chr5:97183178-97183578 | Common:4; Rare:151 |