| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:108569576-108570013 | Common:2; Rare:157 | ||||
| chr7:112206300-112206762 | Common:2; Rare:151 | ||||
| chr7:116499514-116499859 | Common:3; Rare:119 | ||||
| chr7:116499906-116500098 | Common:2; Rare:51 | ||||
| chr7:116524495-116524800 | Rare:72 | ||||
| chr7:116524835-116525159 | Common:3; Rare:104; Clinvar (benign):2 | ||||
| chr7:116526181-116526428 | Common:2; Rare:67 | ||||
| chr7:118184001-118184212 | Common:1; Rare:84 | ||||
| chr7:120950497-120950819 | Common:3; Rare:102 | ||||
| chr7:121396224-121396548 | Common:1; Rare:112 | ||||
| chr7:122144212-122144413 | Common:1; Rare:45 | ||||
| chr7:123534573-123534822 | Common:4; Rare:52 | ||||
| chr7:123557768-123557988 | Common:1; Rare:54 | ||||
| chr7:123748882-123749223 | Common:3; Rare:117 | ||||
| chr7:124929793-124929921 | Common:3; Rare:45 |