| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:160419049-160419171 | Common:2; Rare:38 | ||||
| chr5:163437297-163437628 | Rare:98 | ||||
| chr5:163460046-163460181 | Common:2; Rare:52 | ||||
| chr5:167934585-167934874 | Common:1; Rare:52 | ||||
| chr5:170297716-170297897 | Common:1; Rare:32 | ||||
| chr5:172006509-172006950 | Common:2; Rare:117 | ||||
| chr5:172188194-172188498 | Rare:85 | ||||
| chr5:172770584-172770931 | Common:3; Rare:93 | ||||
| chr5:172771079-172771414 | Common:4; Rare:136 | ||||
| chr5:172834163-172834433 | Common:1; Rare:65 | ||||
| chr5:172958782-172958880 | Rare:26 | ||||
| chr5:172959337-172959490 | Common:2; Rare:56 | ||||
| chr5:172983730-172983957 | Common:1; Rare:84 | ||||
| chr5:173057121-173057394 | Common:1; Rare:73 | ||||
| chr5:173234986-173235068 | Common:2; Rare:33; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 |