| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177497565-177497723 | Rare:63 | ||||
| chr5:177516887-177517093 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177554595-177554733 | Common:1; Rare:42 | ||||
| chr5:177592006-177592280 | Common:2; Rare:102 | ||||
| chr5:177592376-177592669 | Common:1; Rare:86 | ||||
| chr5:177600021-177600224 | Common:4; Rare:68; Clinvar (benign):5 | ||||
| chr5:178153751-178154009 | Rare:85; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204346-178204534 | Common:3; Rare:65 | ||||
| chr5:178232551-178232896 | Common:4; Rare:113 | ||||
| chr5:178626412-178626649 | Common:3; Rare:58 | ||||
| chr5:178859866-178860014 | Common:1; Rare:45 | ||||
| chr5:179023676-179023838 | Common:2; Rare:47 | ||||
| chr5:179060236-179060388 | Common:1; Rare:44 | ||||
| chr5:179559534-179559801 | Common:1; Rare:75 | ||||
| chr5:179623599-179624001 | Common:4; Rare:143 |