| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:7868995-7869205 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr5:9546073-9546361 | Common:7; Rare:68 | ||||
| chr5:10249874-10250180 | Common:16; Rare:143 | ||||
| chr5:10353594-10353913 | Common:3; Rare:117 | ||||
| chr5:10761085-10761458 | Common:13; Rare:120 | ||||
| chr5:16465741-16465887 | Rare:25 | ||||
| chr5:16936251-16936474 | Common:3; Rare:62 | ||||
| chr5:31532043-31532352 | Common:3; Rare:87 | ||||
| chr5:33440606-33441095 | Common:7; Rare:132 | ||||
| chr5:34656158-34656474 | Common:3; Rare:80 | ||||
| chr5:34915216-34915355 | Rare:38 | ||||
| chr5:34915461-34915761 | Common:1; Rare:81 | ||||
| chr5:35617706-35617928 | Common:1; Rare:42 | ||||
| chr5:36151880-36152174 | Rare:91 | ||||
| chr5:36876650-36876885 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 |