| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:9546402-9546517 | Common:3; Rare:18 | ||||
| chr5:10249865-10249937 | Common:13; Rare:76 | ||||
| chr5:10307732-10307781 | Rare:13 | ||||
| chr5:10307789-10308077 | Common:2; Rare:53 | ||||
| chr5:10353578-10353913 | Common:3; Rare:129 | ||||
| chr5:10761085-10761465 | Common:13; Rare:120 | ||||
| chr5:14440945-14441043 | Common:2; Rare:35 | ||||
| chr5:14581637-14581892 | Rare:110 | ||||
| chr5:14664572-14664914 | Common:4; Rare:141 | ||||
| chr5:14871359-14871568 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:16465156-16465949 | Common:1; Rare:238 | ||||
| chr5:16508812-16509121 | Common:2; Rare:52 | ||||
| chr5:16616976-16617182 | Common:2; Rare:58; Clinvar (benign):5 | ||||
| chr5:16935397-16935492 | Rare:25 | ||||
| chr5:16936181-16936447 | Common:3; Rare:79 |