| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:154940974-154941128 | Common:1; Rare:68 | ||||
| chr5:157266009-157266174 | Rare:49 | ||||
| chr5:157460086-157460243 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:159263201-159263337 | Common:1; Rare:45 | ||||
| chr5:160419043-160419154 | Common:2; Rare:36 | ||||
| chr5:163437298-163437623 | Rare:94 | ||||
| chr5:163459971-163460167 | Common:2; Rare:82 | ||||
| chr5:163460372-163460698 | Common:6; Rare:76 | ||||
| chr5:163505442-163505667 | Common:1; Rare:75 | ||||
| chr5:167820459-167820762 | Common:1; Rare:59 | ||||
| chr5:168579292-168579478 | Common:1; Rare:49 | ||||
| chr5:169583592-169583796 | Common:6; Rare:61 | ||||
| chr5:171387512-171388006 | Rare:234; Clinvar:1 | ||||
| chr5:172006491-172006743 | Common:1; Rare:83 | ||||
| chr5:172771171-172771433 | Common:4; Rare:110 |