| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16179789-16179973 | Common:2; Rare:30 | ||||
| chr5:16180711-16180774 | Common:1; Rare:11 | ||||
| chr5:16180785-16180903 | Rare:14 | ||||
| chr5:16465715-16466112 | Common:1; Rare:84 | ||||
| chr5:16616985-16617206 | Common:2; Rare:62; Clinvar (benign):5 | ||||
| chr5:16936131-16936480 | Common:3; Rare:111 | ||||
| chr5:19988177-19988323 | Common:3; Rare:40 | ||||
| chr5:23507289-23507670 | Common:3; Rare:105 | ||||
| chr5:31532032-31532348 | Common:3; Rare:89 | ||||
| chr5:31854778-31855065 | Common:1; Rare:100 | ||||
| chr5:31936070-31936161 | Rare:11 | ||||
| chr5:32174247-32174395 | Common:1; Rare:57 | ||||
| chr5:32444452-32444563 | Rare:32 | ||||
| chr5:32444611-32444868 | Common:1; Rare:96 | ||||
| chr5:32585337-32585621 | Common:2; Rare:102 |