| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177351809-177352038 | Rare:57 | ||||
| chr5:177367024-177367390 | Common:2; Rare:95 | ||||
| chr5:177402744-177402981 | Rare:54 | ||||
| chr5:177425888-177426066 | Rare:46 | ||||
| chr5:177426214-177426546 | Common:2; Rare:104 | ||||
| chr5:177496836-177497074 | Common:3; Rare:53 | ||||
| chr5:177497552-177497870 | Common:1; Rare:116 | ||||
| chr5:177516858-177517093 | Common:2; Rare:97; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177592016-177592213 | Common:1; Rare:64 | ||||
| chr5:177599990-177600159 | Common:3; Rare:51 | ||||
| chr5:178153797-178154172 | Rare:102; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204311-178204535 | Common:3; Rare:78 | ||||
| chr5:178627012-178627239 | Common:7; Rare:79 | ||||
| chr5:178859881-178860114 | Common:3; Rare:66 | ||||
| chr5:178895815-178896174 | Rare:123 |