| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139647739-139647984 | Rare:41 | ||||
| chr5:139648197-139648455 | Common:1; Rare:71 | ||||
| chr5:139648749-139648974 | Rare:62 | ||||
| chr5:140174846-140175281 | Common:1; Rare:122 | ||||
| chr5:140303042-140303191 | Common:1; Rare:50 | ||||
| chr5:140401399-140401918 | Common:3; Rare:118 | ||||
| chr5:140401968-140402267 | Common:1; Rare:90 | ||||
| chr5:140486790-140486929 | Rare:30 | ||||
| chr5:140557396-140557557 | Common:2; Rare:104 | ||||
| chr5:140564282-140564466 | Common:2; Rare:54 | ||||
| chr5:140564543-140564853 | Rare:80 | ||||
| chr5:140639213-140639543 | Common:3; Rare:79 | ||||
| chr5:140647485-140648105 | Common:19; Rare:238; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:140659730-140659762 | Rare:8 | ||||
| chr5:140664750-140664909 | Common:2; Rare:40 |