| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172983696-172983957 | Common:1; Rare:94 | ||||
| chr5:173056145-173056420 | Common:1; Rare:77 | ||||
| chr5:173328381-173328602 | Rare:44 | ||||
| chr5:173917925-173918232 | Common:1; Rare:69 | ||||
| chr5:176061069-176061220 | Common:1; Rare:8 | ||||
| chr5:176112951-176113234 | Common:2; Rare:10 | ||||
| chr5:176238289-176238429 | Common:3; Rare:18 | ||||
| chr5:176361739-176361876 | Rare:40 | ||||
| chr5:176388569-176388822 | Common:4; Rare:103 | ||||
| chr5:176448188-176448409 | Common:1; Rare:78 | ||||
| chr5:177022620-177022746 | Rare:46 | ||||
| chr5:177133488-177133853 | Rare:134 | ||||
| chr5:177134017-177134188 | Common:1; Rare:46 | ||||
| chr5:177303678-177303988 | Common:3; Rare:127 | ||||
| chr5:177516889-177517084 | Common:2; Rare:77; Clinvar:1; Clinvar (pathogenic):1 |