| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:24644717-24644990 | Common:4; Rare:56 | ||||
| chr5:31532048-31532484 | Common:5; Rare:134 | ||||
| chr5:31935954-31936154 | Rare:39 | ||||
| chr5:32174277-32174462 | Common:4; Rare:65 | ||||
| chr5:32444638-32444902 | Common:1; Rare:104 | ||||
| chr5:32585437-32585624 | Common:2; Rare:80 | ||||
| chr5:33440531-33440774 | Common:1; Rare:55 | ||||
| chr5:33440789-33441125 | Common:5; Rare:101 | ||||
| chr5:33441179-33441390 | Common:1; Rare:51 | ||||
| chr5:33461009-33461296 | Common:4; Rare:82 | ||||
| chr5:33891971-33892224 | Rare:52 | ||||
| chr5:34008027-34008231 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656158-34656473 | Common:3; Rare:80 | ||||
| chr5:34839278-34839419 | Common:2; Rare:45 | ||||
| chr5:34915213-34915346 | Rare:37 |