| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138033002-138033193 | Common:1; Rare:70 | ||||
| chr5:138178918-138179190 | Common:3; Rare:56 | ||||
| chr5:138331733-138332101 | Common:2; Rare:96 | ||||
| chr5:138543110-138543490 | Common:2; Rare:114 | ||||
| chr5:138575304-138575667 | Common:2; Rare:146 | ||||
| chr5:138753311-138753503 | Common:2; Rare:61 | ||||
| chr5:139273977-139274130 | Rare:70 | ||||
| chr5:139404072-139404330 | Common:1; Rare:66 | ||||
| chr5:139482707-139482892 | Rare:29 | ||||
| chr5:139561100-139561345 | Common:1; Rare:96 | ||||
| chr5:139561733-139561803 | Rare:28 | ||||
| chr5:140303050-140303165 | Common:1; Rare:39 | ||||
| chr5:140557405-140557530 | Common:1; Rare:79 | ||||
| chr5:140564573-140564857 | Rare:77 | ||||
| chr5:140647588-140648082 | Common:19; Rare:190; Clinvar:4; Clinvar (benign):3 |