| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:134918146-134918354 | Common:4; Rare:63 | ||||
| chr2:134918387-134918931 | Common:3; Rare:229 | ||||
| chr2:134919043-134919312 | Common:2; Rare:70 | ||||
| chr2:134919344-134919509 | Common:3; Rare:42 | ||||
| chr2:135052142-135052358 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:135052531-135052707 | Rare:40 | ||||
| chr2:135530507-135531013 | Common:4; Rare:112 | ||||
| chr2:135531153-135531529 | Common:1; Rare:79 | ||||
| chr2:135531797-135531890 | Rare:22 | ||||
| chr2:135531894-135532058 | Common:2; Rare:56 | ||||
| chr2:135741521-135742023 | Common:5; Rare:164 | ||||
| chr2:135742115-135742199 | Rare:21 | ||||
| chr2:135742310-135742444 | Rare:28 | ||||
| chr2:135742467-135742719 | Rare:56 | ||||
| chr2:135875737-135876025 | Common:1; Rare:74 |