| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1799795-1799988 | Common:4; Rare:92 | ||||
| chr5:1801300-1801460 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:7869000-7869194 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr5:9546046-9546333 | Common:6; Rare:65 | ||||
| chr5:10249879-10250406 | Common:19; Rare:247; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353581-10353908 | Common:3; Rare:123 | ||||
| chr5:14581643-14581841 | Rare:81 | ||||
| chr5:14664567-14664673 | Common:2; Rare:47 | ||||
| chr5:16465734-16465902 | Rare:31 | ||||
| chr5:16713344-16713733 | Common:2; Rare:100 | ||||
| chr5:31532036-31532352 | Common:3; Rare:89 | ||||
| chr5:32174312-32174395 | Common:1; Rare:28 | ||||
| chr5:32444654-32444956 | Common:1; Rare:113 | ||||
| chr5:32585436-32585621 | Common:2; Rare:80 | ||||
| chr5:33440614-33441052 | Common:6; Rare:112 |