| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:173057121-173057406 | Common:1; Rare:74 | ||||
| chr5:173888173-173888353 | Rare:47 | ||||
| chr5:176388550-176388816 | Common:4; Rare:107 | ||||
| chr5:177022600-177022732 | Common:1; Rare:51 | ||||
| chr5:177133488-177133800 | Rare:112 | ||||
| chr5:177134024-177134193 | Common:1; Rare:46 | ||||
| chr5:177303691-177304001 | Common:3; Rare:125 | ||||
| chr5:177311884-177311989 | Common:1; Rare:26 | ||||
| chr5:177351650-177351709 | Rare:16 | ||||
| chr5:177367038-177367325 | Common:2; Rare:71 | ||||
| chr5:177516880-177517100 | Common:2; Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178153771-178154110 | Rare:103; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204339-178204534 | Common:3; Rare:68 | ||||
| chr5:178232572-178232896 | Common:4; Rare:105 | ||||
| chr5:178730612-178730892 | Common:4; Rare:91 |