| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139561728-139561809 | Rare:31 | ||||
| chr5:140303050-140303200 | Common:1; Rare:53 | ||||
| chr5:140346580-140346721 | Common:1; Rare:42 | ||||
| chr5:140401433-140401703 | Common:2; Rare:54 | ||||
| chr5:140557396-140557548 | Common:2; Rare:99 | ||||
| chr5:140564556-140564846 | Rare:76 | ||||
| chr5:140639286-140639515 | Common:3; Rare:60 | ||||
| chr5:140647562-140648084 | Common:19; Rare:201; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664747-140664945 | Common:2; Rare:57 | ||||
| chr5:140691300-140691646 | Common:1; Rare:125; Clinvar:11; Clinvar (benign):1 | ||||
| chr5:141320750-141320890 | Common:1; Rare:41 | ||||
| chr5:141636801-141637011 | Common:2; Rare:95 | ||||
| chr5:141923744-141923904 | Common:1; Rare:42 | ||||
| chr5:142013001-142013142 | Common:1; Rare:41 | ||||
| chr5:142324973-142325296 | Rare:107 |