| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127517373-127517704 | Common:7; Rare:129 | ||||
| chr5:131170817-131171002 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr5:131635211-131635484 | Common:1; Rare:98 | ||||
| chr5:132257488-132257749 | Common:8; Rare:69 | ||||
| chr5:132490750-132490983 | Rare:52 | ||||
| chr5:132777193-132777353 | Common:1; Rare:39 | ||||
| chr5:132866429-132866694 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133051862-133052283 | Rare:141 | ||||
| chr5:133968573-133968722 | Rare:59 | ||||
| chr5:134004510-134004901 | Common:2; Rare:134 | ||||
| chr5:134004913-134005050 | Rare:30 | ||||
| chr5:134226007-134226407 | Common:1; Rare:130 | ||||
| chr5:134371428-134371598 | Common:3; Rare:75 | ||||
| chr5:134411846-134411961 | Rare:43 | ||||
| chr5:134632751-134632937 | Rare:38 |