| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172905013-172905233 | Common:1; Rare:40 | ||||
| chr5:172959362-172959482 | Common:2; Rare:44 | ||||
| chr5:173888178-173888384 | Rare:62 | ||||
| chr5:173890507-173890652 | Rare:41 | ||||
| chr5:176361746-176361896 | Common:1; Rare:44 | ||||
| chr5:176388547-176388816 | Common:4; Rare:109 | ||||
| chr5:176416176-176416460 | Common:1; Rare:90 | ||||
| chr5:176448111-176448410 | Common:1; Rare:107 | ||||
| chr5:176537816-176538127 | Common:1; Rare:97 | ||||
| chr5:177022642-177022774 | Rare:52 | ||||
| chr5:177133476-177133853 | Rare:138 | ||||
| chr5:177303654-177304059 | Common:4; Rare:156 | ||||
| chr5:177497565-177497863 | Common:1; Rare:108 | ||||
| chr5:177516932-177517083 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr5:177553464-177553531 | Rare:19 |