| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:165348332-165348453 | Common:2; Rare:17 | ||||
| chr4:165504674-165504883 | Common:1; Rare:34 | ||||
| chr4:165799680-165799810 | Common:2; Rare:42 | ||||
| chr4:166842241-166842462 | Common:2; Rare:44 | ||||
| chr4:167582122-167582326 | Rare:49 | ||||
| chr4:168616743-168616895 | Rare:33 | ||||
| chr4:168849161-168849203 | Common:1; Rare:8 | ||||
| chr4:168903486-168903891 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:168915639-168915926 | Common:1; Rare:54; Clinvar (benign):2 | ||||
| chr4:168924135-168924420 | Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:169201610-169201737 | Rare:26 | ||||
| chr4:169331024-169331166 | Common:2; Rare:30 | ||||
| chr4:170136781-170136925 | Rare:24 | ||||
| chr4:170226444-170226588 | Common:2; Rare:28 | ||||
| chr4:171043979-171044143 | Common:1; Rare:49 |