| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176388512-176388822 | Common:4; Rare:128 | ||||
| chr5:177022635-177022741 | Rare:39 | ||||
| chr5:177133473-177133813 | Rare:123 | ||||
| chr5:177367030-177367331 | Common:2; Rare:71 | ||||
| chr5:177497547-177497827 | Common:1; Rare:103 | ||||
| chr5:177516925-177517079 | Rare:55; Clinvar (pathogenic):1 | ||||
| chr5:177599970-177600151 | Common:3; Rare:53 | ||||
| chr5:179623629-179623976 | Common:4; Rare:124 | ||||
| chr5:179698649-179699065 | Common:3; Rare:141 | ||||
| chr5:179858798-179858939 | Rare:81 | ||||
| chr5:180353313-180353512 | Common:5; Rare:88 | ||||
| chr5:181223118-181223309 | Rare:64 | ||||
| chr5:181261107-181261286 | Rare:58 | ||||
| chr6:693069-693194 | Rare:40 | ||||
| chr6:2903305-2903399 | Common:2; Rare:21 |