| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:173056163-173056420 | Common:1; Rare:69 | ||||
| chr5:173144385-173144603 | Common:1; Rare:65 | ||||
| chr5:173234959-173235434 | Common:3; Rare:117; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr5:173328336-173328605 | Rare:56 | ||||
| chr5:173917925-173918249 | Common:1; Rare:73 | ||||
| chr5:174724368-174724648 | Common:9; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:175657616-175657798 | Common:1; Rare:34 | ||||
| chr5:175657949-175658127 | Common:2; Rare:56 | ||||
| chr5:176238305-176238443 | Common:4; Rare:20 | ||||
| chr5:176361701-176361969 | Common:3; Rare:76 | ||||
| chr5:176388543-176388901 | Common:5; Rare:141 | ||||
| chr5:176389008-176389384 | Common:2; Rare:118 | ||||
| chr5:176416368-176416761 | Common:1; Rare:106 | ||||
| chr5:176448136-176448410 | Common:1; Rare:93 | ||||
| chr5:176537374-176537620 | Common:5; Rare:66 |