| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134004647-134004850 | Common:1; Rare:75 | ||||
| chr5:134371027-134371274 | Common:1; Rare:63 | ||||
| chr5:134411859-134412036 | Rare:52 | ||||
| chr5:134648569-134648864 | Common:1; Rare:79 | ||||
| chr5:134738423-134738592 | Rare:64 | ||||
| chr5:135578982-135579225 | Common:2; Rare:68 | ||||
| chr5:136365533-136365546 | Rare:1 | ||||
| chr5:138033062-138033170 | Common:1; Rare:37 | ||||
| chr5:138178610-138178776 | Rare:39 | ||||
| chr5:138543214-138543440 | Common:2; Rare:70 | ||||
| chr5:138753288-138753503 | Common:2; Rare:71 | ||||
| chr5:138875289-138875470 | Rare:34; Clinvar (benign):1 | ||||
| chr5:139561733-139561792 | Rare:27 | ||||
| chr5:140564317-140564400 | Rare:25 | ||||
| chr5:140647609-140647911 | Common:5; Rare:120; Clinvar:4; Clinvar (benign):3 |