| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177351793-177352026 | Rare:106 | ||||
| chr5:177370986-177371181 | Common:20; Rare:138 | ||||
| chr5:177379000-177379260 | Rare:61 | ||||
| chr5:177426201-177426950 | Common:6; Rare:350 | ||||
| chr5:177446744-177446844 | Rare:30 | ||||
| chr5:177472711-177473111 | Rare:182 | ||||
| chr5:177497552-177497888 | Common:2; Rare:196 | ||||
| chr5:177516859-177517093 | Common:4; Rare:175; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr5:177554518-177554733 | Common:5; Rare:125 | ||||
| chr5:177592375-177592671 | Common:2; Rare:154 | ||||
| chr5:177599949-177600239 | Common:8; Rare:166; Clinvar (benign):10 | ||||
| chr5:178130811-178131087 | Common:3; Rare:114 | ||||
| chr5:178153737-178154125 | Rare:227; Clinvar:10; Clinvar (benign):3 | ||||
| chr5:178204336-178204659 | Common:9; Rare:234 | ||||
| chr5:178232324-178232425 | Common:1; Rare:46 |