| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:134917786-134918186 | Rare:125 | ||||
| chr2:134918157-134919403 | Common:25; Rare:1381 | ||||
| chr2:135052045-135052445 | Common:8; Rare:398; Clinvar:2; Clinvar (benign):6 | ||||
| chr2:135052457-135052960 | Common:2; Rare:267; Clinvar (pathogenic):6 | ||||
| chr2:135529945-135531080 | Common:22; Rare:724 | ||||
| chr2:135531160-135531772 | Common:7; Rare:628 | ||||
| chr2:135531693-135532093 | Common:3; Rare:145 | ||||
| chr2:135741252-135742931 | Common:28; Rare:1215 | ||||
| chr2:135875784-135876230 | Common:4; Rare:139 | ||||
| chr2:135876330-135876738 | Common:7; Rare:619 | ||||
| chr2:135984739-135985350 | Common:5; Rare:438 | ||||
| chr2:135985404-135986040 | Common:34; Rare:977; Clinvar (benign):7 | ||||
| chr2:137963810-137965151 | Common:22; Rare:714 | ||||
| chr2:138501360-138502045 | Common:24; Rare:1074 | ||||
| chr2:138502060-138502239 | Rare:78 |