| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:112450235-112450465 | Common:4; Rare:72 | ||||
| chr7:116499509-116499859 | Common:3; Rare:121 | ||||
| chr7:116524832-116525092 | Rare:76 | ||||
| chr7:116525247-116525531 | Common:3; Rare:84 | ||||
| chr7:117872190-117872388 | Common:3; Rare:42 | ||||
| chr7:118184000-118184217 | Common:1; Rare:87 | ||||
| chr7:120950509-120950839 | Common:2; Rare:102 | ||||
| chr7:122144196-122144444 | Common:1; Rare:53 | ||||
| chr7:123534554-123534814 | Common:4; Rare:55 | ||||
| chr7:123748920-123749276 | Common:3; Rare:131 | ||||
| chr7:124929792-124929915 | Common:3; Rare:41 | ||||
| chr7:124929937-124929967 | Rare:9 | ||||
| chr7:127651820-127652227 | Common:3; Rare:119 | ||||
| chr7:128409843-128410094 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455743-128455919 | Common:2; Rare:103 |