| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32532276-32532566 | Common:1; Rare:41 | ||||
| chr5:32585546-32585675 | Common:2; Rare:51 | ||||
| chr5:32585981-32586259 | Common:3; Rare:101 | ||||
| chr5:32586268-32586536 | Common:4; Rare:59 | ||||
| chr5:33440539-33441132 | Common:7; Rare:164 | ||||
| chr5:33441134-33441168 | Rare:10 | ||||
| chr5:33441170-33441448 | Common:1; Rare:70 | ||||
| chr5:34007638-34008531 | Common:7; Rare:267; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr5:34839031-34839392 | Common:2; Rare:126 | ||||
| chr5:34915211-34915366 | Rare:41 | ||||
| chr5:34915411-34915836 | Common:1; Rare:123 | ||||
| chr5:34929236-34929681 | Common:2; Rare:125 | ||||
| chr5:34929829-34930066 | Common:1; Rare:63 | ||||
| chr5:35230453-35230487 | Rare:6 | ||||
| chr5:35617702-35617928 | Common:1; Rare:43 |