| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:154857827-154857889 | Rare:18 | ||||
| chr5:154858468-154858714 | Common:1; Rare:79 | ||||
| chr5:154938186-154938239 | Rare:14 | ||||
| chr5:157266072-157266177 | Rare:39 | ||||
| chr5:157859043-157859288 | Common:2; Rare:69 | ||||
| chr5:159263201-159263330 | Common:1; Rare:43 | ||||
| chr5:160400032-160400189 | Common:1; Rare:47 | ||||
| chr5:160419031-160419171 | Common:2; Rare:46 | ||||
| chr5:163437292-163437628 | Rare:99 | ||||
| chr5:163460026-163460175 | Common:2; Rare:62 | ||||
| chr5:163460312-163460672 | Common:5; Rare:82 | ||||
| chr5:163505444-163505661 | Common:1; Rare:72 | ||||
| chr5:168486305-168486497 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr5:169583588-169583796 | Common:6; Rare:68 | ||||
| chr5:171387061-171387115 | Rare:14 |