| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:121396281-121396586 | Common:2; Rare:189 | ||||
| chr7:122886403-122886848 | Common:2; Rare:189 | ||||
| chr7:123557779-123558036 | Common:1; Rare:108 | ||||
| chr7:123748630-123748870 | Common:1; Rare:96 | ||||
| chr7:123748838-123749274 | Common:6; Rare:287 | ||||
| chr7:124929775-124930113 | Common:6; Rare:163 | ||||
| chr7:127392538-127392833 | Common:5; Rare:116 | ||||
| chr7:127585552-127585734 | Common:5; Rare:127 | ||||
| chr7:127588265-127588488 | Rare:161 | ||||
| chr7:127588899-127589138 | Rare:117 | ||||
| chr7:127651788-127652295 | Common:6; Rare:296 | ||||
| chr7:127686251-127686880 | Rare:222 | ||||
| chr7:128343805-128344028 | Common:4; Rare:61 | ||||
| chr7:128405919-128406069 | Common:2; Rare:61 | ||||
| chr7:128409913-128410013 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):1 |