| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:53560434-53560754 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:54310434-54310711 | Common:1; Rare:82 | ||||
| chr5:55233606-55233862 | Common:4; Rare:87 | ||||
| chr5:55307597-55308064 | Common:5; Rare:174 | ||||
| chr5:56815196-56815526 | Common:2; Rare:120 | ||||
| chr5:57173518-57174136 | Common:3; Rare:225 | ||||
| chr5:58459983-58460192 | Common:5; Rare:90 | ||||
| chr5:60488061-60488336 | Rare:48 | ||||
| chr5:60700048-60700237 | Common:1; Rare:72 | ||||
| chr5:60844175-60844464 | Common:5; Rare:96 | ||||
| chr5:60945026-60945245 | Common:5; Rare:84; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162339-61162637 | Common:1; Rare:77 | ||||
| chr5:62403821-62404044 | Common:3; Rare:78 | ||||
| chr5:62412545-62412786 | Rare:76 | ||||
| chr5:64165532-64165924 | Common:2; Rare:126 |