| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172454354-172454661 | Common:10; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172770256-172770776 | Common:5; Rare:142 | ||||
| chr5:172771049-172771485 | Common:5; Rare:161 | ||||
| chr5:172834162-172834419 | Common:1; Rare:62 | ||||
| chr5:172958597-172958925 | Common:3; Rare:105 | ||||
| chr5:172959288-172959530 | Common:3; Rare:79 | ||||
| chr5:173328088-173328596 | Common:1; Rare:118 | ||||
| chr5:173329565-173329592 | Rare:2 | ||||
| chr5:173616226-173616346 | Rare:22 | ||||
| chr5:173888683-173889066 | Common:1; Rare:63 | ||||
| chr5:176361729-176361896 | Common:1; Rare:51 | ||||
| chr5:176388500-176388784 | Common:2; Rare:106 | ||||
| chr5:176388940-176389214 | Common:1; Rare:82 | ||||
| chr5:176448193-176448405 | Common:1; Rare:77 | ||||
| chr5:176906011-176906084 | Rare:22 |