| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138753249-138753507 | Common:2; Rare:88 | ||||
| chr5:139198280-139198531 | Rare:83; Clinvar (benign):1 | ||||
| chr5:139273969-139274140 | Rare:80 | ||||
| chr5:139482658-139482944 | Rare:42 | ||||
| chr5:139561131-139561425 | Common:1; Rare:121 | ||||
| chr5:139561727-139561813 | Rare:33 | ||||
| chr5:139648216-139648368 | Rare:45 | ||||
| chr5:140107696-140107815 | Rare:34 | ||||
| chr5:140303069-140303160 | Common:1; Rare:25 | ||||
| chr5:140346563-140346827 | Common:1; Rare:76 | ||||
| chr5:140401433-140401912 | Common:3; Rare:111 | ||||
| chr5:140547610-140547730 | Common:1; Rare:29 | ||||
| chr5:140557405-140557584 | Common:3; Rare:102 | ||||
| chr5:140564305-140564858 | Common:1; Rare:139 | ||||
| chr5:140647576-140647924 | Common:5; Rare:143; Clinvar:4; Clinvar (benign):3 |