| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16508804-16509067 | Common:1; Rare:47 | ||||
| chr5:16936256-16936498 | Common:3; Rare:70 | ||||
| chr5:24644717-24644871 | Common:4; Rare:29 | ||||
| chr5:31532037-31532356 | Common:3; Rare:88 | ||||
| chr5:32174276-32174427 | Common:2; Rare:53 | ||||
| chr5:32585484-32585623 | Common:2; Rare:65 | ||||
| chr5:33440611-33441076 | Common:6; Rare:122 | ||||
| chr5:33891965-33892289 | Rare:75 | ||||
| chr5:34008006-34008222 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34839264-34839448 | Common:3; Rare:54 | ||||
| chr5:34915461-34915741 | Common:1; Rare:68 | ||||
| chr5:34929686-34929987 | Rare:98 | ||||
| chr5:36151774-36152190 | Rare:110 | ||||
| chr5:36241624-36241738 | Rare:31; Clinvar (benign):1 | ||||
| chr5:36242096-36242334 | Common:2; Rare:64; Clinvar (benign):1 |