| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:2354006-2354117 | Common:2; Rare:57 | ||||
| chr7:2354190-2354959 | Common:11; Rare:487 | ||||
| chr7:2403271-2403637 | Common:2; Rare:279 | ||||
| chr7:2519524-2519802 | Common:4; Rare:252 | ||||
| chr7:2631609-2632049 | Common:5; Rare:232 | ||||
| chr7:2844188-2844913 | Common:10; Rare:392 | ||||
| chr7:4682081-4682321 | Common:2; Rare:174 | ||||
| chr7:4775387-4775737 | Common:14; Rare:323; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:5045734-5045962 | Common:7; Rare:175 | ||||
| chr7:5190113-5190315 | Rare:164 | ||||
| chr7:5423648-5424068 | Common:8; Rare:203 | ||||
| chr7:5425858-5426058 | Rare:56 | ||||
| chr7:5513728-5513897 | Common:2; Rare:135 | ||||
| chr7:5514060-5514400 | Common:3; Rare:80 | ||||
| chr7:5530525-5530807 | Common:1; Rare:157; Clinvar (benign):4 |