| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15478970-15479283 | Common:2; Rare:70 | ||||
| chr4:15655258-15655477 | Common:2; Rare:91 | ||||
| chr4:15681421-15681906 | Common:4; Rare:161 | ||||
| chr4:16898404-16898704 | Rare:65 | ||||
| chr4:17614532-17614651 | Common:2; Rare:46 | ||||
| chr4:17810598-17811080 | Common:4; Rare:145 | ||||
| chr4:20700337-20700480 | Rare:66 | ||||
| chr4:24584321-24584716 | Common:1; Rare:126 | ||||
| chr4:25160347-25160740 | Common:3; Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233835-25234094 | Rare:106 | ||||
| chr4:25914051-25914340 | Common:3; Rare:124 | ||||
| chr4:26320590-26320832 | Common:1; Rare:92 | ||||
| chr4:26320905-26321046 | Rare:51; Clinvar (benign):1 | ||||
| chr4:26860568-26860793 | Common:1; Rare:70 | ||||
| chr4:30719966-30720096 | Common:1; Rare:24 |