| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106284978-106285262 | Common:2; Rare:104 | ||||
| chr7:106285540-106285712 | Rare:41 | ||||
| chr7:107563873-107563996 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:107580217-107580294 | Rare:31 | ||||
| chr7:107744053-107744159 | Rare:36 | ||||
| chr7:108569601-108569931 | Common:1; Rare:110 | ||||
| chr7:111090851-111091154 | Rare:54 | ||||
| chr7:112206384-112206712 | Common:1; Rare:106 | ||||
| chr7:116499572-116499748 | Common:3; Rare:62 | ||||
| chr7:116524828-116525089 | Rare:75 | ||||
| chr7:116526180-116526368 | Common:2; Rare:59 | ||||
| chr7:118183982-118184194 | Common:2; Rare:79 | ||||
| chr7:122144217-122144396 | Common:1; Rare:37 | ||||
| chr7:123748942-123749214 | Common:3; Rare:96 | ||||
| chr7:124929800-124929883 | Common:2; Rare:23 |