| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:160009025-160009188 | Common:1; Rare:37 | ||||
| chr5:160419053-160419195 | Common:2; Rare:52 | ||||
| chr5:160421680-160421956 | Common:1; Rare:80 | ||||
| chr5:163437316-163437612 | Rare:87 | ||||
| chr5:163459795-163459890 | Rare:33 | ||||
| chr5:163460326-163460695 | Common:6; Rare:89 | ||||
| chr5:163505482-163505642 | Rare:46 | ||||
| chr5:168486337-168486490 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr5:168579617-168579938 | Common:2; Rare:80 | ||||
| chr5:169583609-169583816 | Common:6; Rare:66 | ||||
| chr5:169637015-169637318 | Common:3; Rare:62 | ||||
| chr5:171387482-171388006 | Common:1; Rare:242; Clinvar:1 | ||||
| chr5:172006564-172006669 | Common:1; Rare:39 | ||||
| chr5:172188190-172188532 | Common:1; Rare:91 | ||||
| chr5:172834163-172834423 | Common:1; Rare:64 |