| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:136033423-136033425 | |||||
| chr3:136165755-136166211 | Common:2; Rare:100 | ||||
| chr3:136326697-136326852 | Rare:34; Clinvar:1 | ||||
| chr3:136329674-136329912 | Rare:48; Clinvar (benign):1 | ||||
| chr3:136332567-136332676 | Common:1; Rare:25 | ||||
| chr3:136333292-136333327 | Rare:6 | ||||
| chr3:136409797-136410060 | Rare:34 | ||||
| chr3:136411795-136411903 | Common:1; Rare:19 | ||||
| chr3:136430637-136430789 | Rare:24 | ||||
| chr3:136595542-136595587 | Rare:7 | ||||
| chr3:136600146-136600336 | Rare:35 | ||||
| chr3:136650947-136650982 | Rare:7 | ||||
| chr3:136678912-136678988 | Rare:8 | ||||
| chr3:136751386-136751553 | Common:1; Rare:60 | ||||
| chr3:136751580-136751715 | Common:1; Rare:33 |