| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141014930-141015046 | Rare:26 | ||||
| chr7:141551330-141551428 | Rare:30; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738464 | Common:4; Rare:132 | ||||
| chr7:143382113-143382182 | Rare:16 | ||||
| chr7:144835974-144836053 | Common:1; Rare:19; Clinvar (benign):1 | ||||
| chr7:148698575-148698949 | Common:3; Rare:134 | ||||
| chr7:149090656-149090915 | Rare:73 | ||||
| chr7:149126278-149126445 | Common:5; Rare:54 | ||||
| chr7:150632310-150632562 | Common:2; Rare:40 | ||||
| chr7:150737279-150737640 | Common:7; Rare:88 | ||||
| chr7:150800321-150800447 | Common:2; Rare:29 | ||||
| chr7:151080793-151080962 | Rare:51 | ||||
| chr7:151232246-151232537 | Common:2; Rare:92 | ||||
| chr7:151633081-151633281 | Common:1; Rare:31 | ||||
| chr7:152025583-152025774 | Rare:78 |