| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132866414-132866698 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963331-132963632 | Common:3; Rare:84 | ||||
| chr5:133026504-133026772 | Common:5; Rare:71 | ||||
| chr5:133051851-133052222 | Rare:128 | ||||
| chr5:133968573-133968696 | Rare:57 | ||||
| chr5:134004647-134004838 | Common:1; Rare:72 | ||||
| chr5:134004933-134005111 | Rare:37 | ||||
| chr5:134176917-134177295 | Common:3; Rare:117 | ||||
| chr5:134225526-134225638 | Common:1; Rare:43 | ||||
| chr5:134371395-134371589 | Common:3; Rare:84 | ||||
| chr5:134411846-134412036 | Rare:61 | ||||
| chr5:134632744-134632918 | Rare:36 | ||||
| chr5:134648662-134648816 | Rare:44 | ||||
| chr5:134738281-134738609 | Rare:113 | ||||
| chr5:134758556-134758826 | Common:2; Rare:95 |