| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:127651862-127652174 | Common:2; Rare:78 | ||||
| chr7:128862963-128863060 | Common:1; Rare:16 | ||||
| chr7:129054883-129055226 | Common:2; Rare:66 | ||||
| chr7:129611623-129611813 | Common:1; Rare:59 | ||||
| chr7:131109892-131110112 | Common:1; Rare:36 | ||||
| chr7:131327670-131327912 | Rare:74 | ||||
| chr7:134646595-134646853 | Common:5; Rare:72 | ||||
| chr7:135148033-135148104 | Rare:19 | ||||
| chr7:135170678-135170927 | Common:3; Rare:89 | ||||
| chr7:135977032-135977216 | Rare:55 | ||||
| chr7:139035985-139036229 | Rare:71 | ||||
| chr7:139778013-139778269 | Common:1; Rare:62 | ||||
| chr7:140176939-140177179 | Common:2; Rare:79 | ||||
| chr7:140697079-140697286 | Rare:64 | ||||
| chr7:141551246-141551439 | Common:2; Rare:52; Clinvar:5; Clinvar (benign):2 |