| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183987578-183987828 | Common:1; Rare:49 | ||||
| chr4:183988132-183988332 | Rare:30 | ||||
| chr4:184343905-184344073 | Rare:32 | ||||
| chr4:184537535-184537632 | Common:2; Rare:19 | ||||
| chr4:184815069-184815254 | Common:2; Rare:43 | ||||
| chr4:185127836-185128165 | Common:3; Rare:89 | ||||
| chr4:185504509-185504701 | Common:1; Rare:61; Clinvar:4; Clinvar (benign):4 | ||||
| chr4:185606511-185606621 | Rare:16 | ||||
| chr4:185665505-185665797 | Common:4; Rare:44 | ||||
| chr4:185665917-185666009 | Common:1; Rare:21 | ||||
| chr4:185794628-185794768 | Rare:17 | ||||
| chr4:185878648-185878920 | Common:2; Rare:39 | ||||
| chr5:82226-82375 | Common:1; Rare:33 | ||||
| chr5:91951-92214 | Rare:90 | ||||
| chr5:194200-194234 | Rare:4 |