| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:159207908-159208165 | Common:2; Rare:56 | ||||
| chr5:159263244-159263326 | Common:1; Rare:24 | ||||
| chr5:160400043-160400207 | Common:3; Rare:46 | ||||
| chr5:160419049-160419262 | Common:4; Rare:81 | ||||
| chr5:163460376-163460664 | Common:5; Rare:61 | ||||
| chr5:168579290-168579454 | Common:1; Rare:42 | ||||
| chr5:172188190-172188499 | Common:1; Rare:86 | ||||
| chr5:172959311-172959460 | Common:2; Rare:53 | ||||
| chr5:176448188-176448407 | Common:1; Rare:78 | ||||
| chr5:177022600-177022743 | Common:1; Rare:58 | ||||
| chr5:177303654-177303843 | Common:4; Rare:96 | ||||
| chr5:177351647-177351731 | Rare:22 | ||||
| chr5:177516875-177517048 | Common:2; Rare:76; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178232792-178232987 | Common:1; Rare:69 | ||||
| chr5:179023639-179023834 | Common:3; Rare:53 |