| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10249875-10250170 | Common:16; Rare:141 | ||||
| chr5:10353578-10353905 | Common:3; Rare:125 | ||||
| chr5:14479127-14479329 | Common:3; Rare:53 | ||||
| chr5:16465538-16465882 | Rare:91 | ||||
| chr5:31532045-31532352 | Common:3; Rare:87 | ||||
| chr5:32174252-32174389 | Common:1; Rare:54 | ||||
| chr5:33440632-33441116 | Common:7; Rare:139 | ||||
| chr5:34686776-34686916 | Common:1; Rare:27 | ||||
| chr5:34915450-34915766 | Common:1; Rare:88 | ||||
| chr5:35230459-35230525 | Rare:11 | ||||
| chr5:36151819-36152174 | Rare:99 | ||||
| chr5:36876657-36876889 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36876993-36877159 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37058652-37058936 | Rare:64; Clinvar:1 | ||||
| chr5:37379057-37379364 | Common:3; Rare:72 |