| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184323938-184324237 | Common:2; Rare:72 | ||||
| chr3:184710434-184710457 | Rare:5 | ||||
| chr3:185919448-185919530 | Rare:17 | ||||
| chr3:195692255-195692434 | Common:3; Rare:14 | ||||
| chr3:197627841-197628064 | Common:8; Rare:85 | ||||
| chr4:672464-672585 | Common:1; Rare:41 | ||||
| chr4:6673855-6674085 | Common:11; Rare:108 | ||||
| chr4:10074286-10074345 | Common:1; Rare:12 | ||||
| chr4:10103776-10103979 | Common:2; Rare:66 | ||||
| chr4:14111963-14112108 | Common:2; Rare:38 | ||||
| chr4:38868349-38868452 | Rare:18 | ||||
| chr4:38905607-38905845 | Rare:78 | ||||
| chr4:39300135-39300411 | Common:1; Rare:78 | ||||
| chr4:54231865-54232074 | Common:2; Rare:48 | ||||
| chr4:56490357-56490595 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):3 |