| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134226022-134226410 | Common:1; Rare:124 | ||||
| chr5:134371027-134371208 | Common:1; Rare:46 | ||||
| chr5:134411852-134412006 | Rare:50 | ||||
| chr5:134648721-134648890 | Rare:44 | ||||
| chr5:134738493-134738675 | Common:1; Rare:80 | ||||
| chr5:136029054-136029189 | Rare:47 | ||||
| chr5:138178603-138178911 | Rare:59 | ||||
| chr5:138178935-138179201 | Common:3; Rare:53 | ||||
| chr5:138331783-138332108 | Common:2; Rare:80 | ||||
| chr5:138543096-138543535 | Common:2; Rare:135 | ||||
| chr5:139561696-139561804 | Rare:41 | ||||
| chr5:140174994-140175247 | Rare:71 | ||||
| chr5:140401550-140401878 | Common:1; Rare:67 | ||||
| chr5:140564303-140564871 | Common:1; Rare:142 | ||||
| chr5:140647579-140647880 | Common:5; Rare:124; Clinvar:4; Clinvar (benign):3 |