| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303691-177303976 | Common:3; Rare:119 | ||||
| chr5:177312287-177312520 | Rare:71 | ||||
| chr5:177516932-177517084 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr5:178130831-178131026 | Rare:55 | ||||
| chr5:178153828-178154170 | Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:179623614-179623976 | Common:4; Rare:131 | ||||
| chr5:179698610-179699072 | Common:3; Rare:166 | ||||
| chr5:179858797-179858977 | Rare:100 | ||||
| chr5:180330876-180331137 | Common:3; Rare:56 | ||||
| chr5:180353305-180353545 | Common:7; Rare:105 | ||||
| chr5:180802775-180803007 | Common:8; Rare:82 | ||||
| chr5:180861216-180861397 | Common:2; Rare:75 | ||||
| chr5:181223116-181223313 | Rare:68 | ||||
| chr5:181223589-181223752 | Common:3; Rare:39 | ||||
| chr5:181243801-181244240 | Common:10; Rare:140 |