| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:6378492-6378707 | Rare:90 | ||||
| chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr5:9546074-9546313 | Common:6; Rare:55 | ||||
| chr5:10249847-10250436 | Common:19; Rare:276; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353578-10353901 | Common:3; Rare:125 | ||||
| chr5:14581643-14581873 | Rare:101 | ||||
| chr5:16465709-16465882 | Rare:30 | ||||
| chr5:16741886-16742020 | Rare:22 | ||||
| chr5:31532045-31532407 | Common:4; Rare:107 | ||||
| chr5:31854844-31855113 | Common:2; Rare:100 | ||||
| chr5:32173819-32173955 | Rare:43 | ||||
| chr5:32174267-32174328 | Common:1; Rare:23 | ||||
| chr5:33440611-33440765 | Common:1; Rare:32 | ||||
| chr5:33440791-33441134 | Common:5; Rare:104 | ||||
| chr5:33891967-33892257 | Rare:64 |