| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:116862842-116862984 | Rare:33 | ||||
| chr7:116953300-116953536 | Common:2; Rare:66 | ||||
| chr7:118183965-118184238 | Common:2; Rare:105 | ||||
| chr7:120950502-120950833 | Common:2; Rare:104 | ||||
| chr7:120988687-120988749 | Rare:9 | ||||
| chr7:122144181-122144433 | Common:1; Rare:52 | ||||
| chr7:123748641-123749285 | Common:4; Rare:230 | ||||
| chr7:124929792-124929919 | Common:3; Rare:44 | ||||
| chr7:127585580-127585686 | Common:2; Rare:35 | ||||
| chr7:127588291-127588530 | Rare:98 | ||||
| chr7:127651830-127652235 | Common:3; Rare:120 | ||||
| chr7:127990883-127990987 | Rare:16 | ||||
| chr7:128405916-128406141 | Common:2; Rare:81 | ||||
| chr7:128409884-128410044 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455760-128455961 | Common:2; Rare:118 |