| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6425046-6425250 | Common:4; Rare:55 | ||||
| chr7:6503640-6503812 | Common:1; Rare:54 | ||||
| chr7:6953954-6954019 | Common:1; Rare:19 | ||||
| chr7:6991052-6991289 | Common:4; Rare:56 | ||||
| chr7:7566031-7566223 | Common:1; Rare:35 | ||||
| chr7:16989933-16990321 | Common:2; Rare:83 | ||||
| chr7:17642533-17642788 | Common:2; Rare:51 | ||||
| chr7:21908436-21908773 | Common:2; Rare:82 | ||||
| chr7:23680815-23680931 | Common:2; Rare:27 | ||||
| chr7:26193546-26193960 | Rare:152; Clinvar (benign):2 | ||||
| chr7:26194500-26194503 | Rare:1 | ||||
| chr7:26194605-26194864 | Common:5; Rare:105 | ||||
| chr7:26194895-26194967 | Rare:18 | ||||
| chr7:26195015-26195068 | Common:1; Rare:18 | ||||
| chr7:26199928-26199953 | Rare:9 |