| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69166927-69167168 | Common:1; Rare:55 | ||||
| chr5:69189464-69189560 | Common:1; Rare:28 | ||||
| chr5:69332739-69332855 | Rare:32 | ||||
| chr5:69369473-69370067 | Common:3; Rare:205 | ||||
| chr5:71456016-71456083 | Rare:25 | ||||
| chr5:72107154-72107715 | Common:2; Rare:198 | ||||
| chr5:72179431-72179810 | Common:1; Rare:80 | ||||
| chr5:72816546-72816740 | Common:3; Rare:77 | ||||
| chr5:72955860-72956085 | Common:1; Rare:102 | ||||
| chr5:73498305-73498558 | Common:3; Rare:83 | ||||
| chr5:73565365-73565812 | Common:7; Rare:137 | ||||
| chr5:74685119-74685380 | Common:2; Rare:96; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:74767045-74767363 | Common:3; Rare:102 | ||||
| chr5:75336919-75337270 | Common:3; Rare:119 | ||||
| chr5:75511610-75511913 | Common:1; Rare:112 |