| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303942-177304077 | Rare:34 | ||||
| chr5:177311869-177312005 | Common:1; Rare:40 | ||||
| chr5:177312265-177312530 | Rare:83 | ||||
| chr5:177351629-177351772 | Rare:41 | ||||
| chr5:177371044-177371185 | Common:19; Rare:116 | ||||
| chr5:177402817-177402928 | Rare:22 | ||||
| chr5:177404423-177404604 | Common:2; Rare:58; Clinvar (benign):2 | ||||
| chr5:177447882-177448055 | Common:2; Rare:35 | ||||
| chr5:177497550-177497865 | Common:1; Rare:116 | ||||
| chr5:177516881-177517100 | Common:2; Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177600021-177600243 | Common:4; Rare:74; Clinvar (benign):5 | ||||
| chr5:178130868-178131040 | Rare:44 | ||||
| chr5:178153797-178154110 | Rare:92; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204337-178204537 | Common:3; Rare:69 | ||||
| chr5:178204694-178204993 | Common:1; Rare:76 |