| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32585966-32586101 | Common:1; Rare:51 | ||||
| chr5:32586204-32586492 | Common:4; Rare:68 | ||||
| chr5:33440593-33441057 | Common:6; Rare:119 | ||||
| chr5:33892624-33892648 | Rare:4 | ||||
| chr5:34008009-34008214 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656159-34656430 | Common:3; Rare:66 | ||||
| chr5:34684034-34684279 | Common:3; Rare:46 | ||||
| chr5:34684421-34684680 | Rare:36 | ||||
| chr5:34687404-34687591 | Common:2; Rare:26 | ||||
| chr5:34838713-34838856 | Common:3; Rare:31 | ||||
| chr5:34839082-34839196 | Rare:40 | ||||
| chr5:34839201-34839457 | Common:3; Rare:81 | ||||
| chr5:34915212-34915307 | Rare:26 | ||||
| chr5:34915437-34915852 | Common:2; Rare:121 | ||||
| chr5:34929457-34929907 | Rare:159 |