| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:170389631-170389968 | Common:2; Rare:58 | ||||
| chr5:172454366-172454699 | Common:12; Rare:91; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172770579-172770931 | Common:3; Rare:94 | ||||
| chr5:172770986-172771164 | Rare:49 | ||||
| chr5:172771167-172771433 | Common:4; Rare:113 | ||||
| chr5:172834163-172834429 | Common:1; Rare:65 | ||||
| chr5:173056148-173056415 | Common:1; Rare:74 | ||||
| chr5:173328412-173328596 | Rare:34 | ||||
| chr5:173890428-173890636 | Rare:58 | ||||
| chr5:175657679-175657797 | Common:1; Rare:24 | ||||
| chr5:176361739-176361896 | Common:1; Rare:47 | ||||
| chr5:176388550-176388809 | Common:4; Rare:102 | ||||
| chr5:176448162-176448427 | Common:1; Rare:95 | ||||
| chr5:177022635-177022741 | Rare:39 | ||||
| chr5:177133461-177133848 | Rare:142 |