| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:151758602-151758851 | Common:2; Rare:79 | ||||
| chr5:151770695-151770902 | Common:1; Rare:75 | ||||
| chr5:151771987-151772604 | Common:3; Rare:203 | ||||
| chr5:151924142-151924542 | Rare:162; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:153490945-153491345 | Common:2; Rare:108 | ||||
| chr5:153491565-153492102 | Common:3; Rare:160 | ||||
| chr5:153572730-153573100 | Common:5; Rare:70 | ||||
| chr5:154038822-154039014 | Common:1; Rare:63 | ||||
| chr5:154190409-154190769 | Common:1; Rare:113 | ||||
| chr5:154287240-154287520 | Common:1; Rare:45 | ||||
| chr5:154445768-154446009 | Common:1; Rare:76 | ||||
| chr5:154754956-154755357 | Common:4; Rare:133 | ||||
| chr5:154756720-154757183 | Common:4; Rare:178 | ||||
| chr5:154757182-154757646 | Common:6; Rare:181 | ||||
| chr5:154850568-154850760 | Common:1; Rare:35 |