| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:7869000-7869200 | Common:2; Rare:100; Clinvar (benign):1 | ||||
| chr5:9546073-9546362 | Common:7; Rare:68 | ||||
| chr5:10353597-10353913 | Common:3; Rare:115 | ||||
| chr5:16465732-16465882 | Rare:25 | ||||
| chr5:16616973-16617202 | Common:2; Rare:65; Clinvar (benign):5 | ||||
| chr5:31532037-31532367 | Common:3; Rare:95 | ||||
| chr5:31936027-31936161 | Rare:21 | ||||
| chr5:32173819-32174120 | Rare:93 | ||||
| chr5:32174277-32174328 | Common:1; Rare:19 | ||||
| chr5:32710581-32710688 | Common:1; Rare:26 | ||||
| chr5:33440632-33441108 | Common:7; Rare:136 | ||||
| chr5:34656158-34656473 | Common:3; Rare:80 | ||||
| chr5:34929536-34929851 | Rare:121 | ||||
| chr5:35617712-35617928 | Common:1; Rare:41 | ||||
| chr5:35856803-35856995 | Rare:40 |