| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16936227-16936498 | Common:3; Rare:85 | ||||
| chr5:31532052-31532332 | Common:3; Rare:76 | ||||
| chr5:32173953-32174120 | Rare:49 | ||||
| chr5:32174247-32174351 | Common:1; Rare:42 | ||||
| chr5:33440611-33441117 | Common:7; Rare:141 | ||||
| chr5:34915472-34915733 | Common:1; Rare:63 | ||||
| chr5:34929605-34929897 | Rare:102 | ||||
| chr5:35047864-35048011 | Rare:46 | ||||
| chr5:35617665-35617921 | Common:1; Rare:47 | ||||
| chr5:35856803-35857059 | Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36151792-36152140 | Rare:84 | ||||
| chr5:36241649-36241909 | Common:4; Rare:90; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:36242162-36242350 | Common:1; Rare:49 | ||||
| chr5:36876627-36876915 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371024-37371245 | Rare:74 |