| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:150323527-150323595 | Rare:15 | ||||
| chr7:150341571-150342006 | Common:2; Rare:70 | ||||
| chr7:150379045-150379365 | Common:2; Rare:118 | ||||
| chr7:150450538-150450765 | Common:1; Rare:44 | ||||
| chr7:150632254-150632548 | Common:3; Rare:51 | ||||
| chr7:150716432-150716641 | Common:2; Rare:38 | ||||
| chr7:150737274-150737654 | Common:7; Rare:93 | ||||
| chr7:150799896-150800060 | Common:2; Rare:34 | ||||
| chr7:150800307-150800449 | Common:3; Rare:35 | ||||
| chr7:150800471-150800836 | Common:3; Rare:88 | ||||
| chr7:150978292-150978565 | Common:4; Rare:76 | ||||
| chr7:151028218-151028490 | Rare:104 | ||||
| chr7:151057856-151058148 | Common:3; Rare:85 | ||||
| chr7:151080785-151080928 | Rare:41 | ||||
| chr7:151187128-151187337 | Common:3; Rare:56; Clinvar (benign):1 |