| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100895860-100896060 | Rare:39 | ||||
| chr7:101085317-101085521 | Common:2; Rare:70 | ||||
| chr7:101126350-101126700 | Common:8; Rare:161; Clinvar (pathogenic):2 | ||||
| chr7:101126968-101127110 | Common:1; Rare:29 | ||||
| chr7:101200961-101201443 | Common:2; Rare:121 | ||||
| chr7:101217849-101218201 | Common:4; Rare:113 | ||||
| chr7:101245009-101245198 | Common:2; Rare:150 | ||||
| chr7:101252237-101252509 | Common:1; Rare:105 | ||||
| chr7:101321690-101321990 | Common:6; Rare:144 | ||||
| chr7:101362542-101362914 | Common:3; Rare:101 | ||||
| chr7:101815548-101816055 | Common:6; Rare:275 | ||||
| chr7:102273870-102274270 | Common:4; Rare:131 | ||||
| chr7:102286608-102287008 | Common:14; Rare:173 | ||||
| chr7:102363677-102363964 | Common:1; Rare:84 | ||||
| chr7:102433431-102433624 | Common:2; Rare:87 |