| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176609724-176609903 | Common:2; Rare:55 | ||||
| chr5:176610000-176610390 | Common:3; Rare:124 | ||||
| chr5:176630431-176630831 | Common:5; Rare:152 | ||||
| chr5:176647139-176647503 | Common:4; Rare:112 | ||||
| chr5:176883685-176884085 | Common:2; Rare:219; Clinvar (benign):1 | ||||
| chr5:177006530-177006898 | Common:4; Rare:109 | ||||
| chr5:177022553-177022760 | Common:1; Rare:85 | ||||
| chr5:177133559-177133959 | Rare:186; Clinvar:1 | ||||
| chr5:177134480-177134830 | Common:2; Rare:83 | ||||
| chr5:177303655-177303816 | Common:4; Rare:76 | ||||
| chr5:177311884-177312054 | Common:1; Rare:45 | ||||
| chr5:177312198-177312520 | Common:1; Rare:94 | ||||
| chr5:177351620-177351794 | Rare:47 | ||||
| chr5:177351822-177352065 | Rare:63 | ||||
| chr5:177366990-177367460 | Common:2; Rare:122 |