| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130182109-130182381 | Common:2; Rare:107 | ||||
| chr2:130342118-130342228 | Rare:45; Clinvar:1 | ||||
| chr2:131105192-131105375 | Common:1; Rare:84 | ||||
| chr2:131492754-131493119 | Common:8; Rare:111 | ||||
| chr2:132416425-132416631 | Common:1; Rare:54 | ||||
| chr2:134838520-134838655 | Rare:29 | ||||
| chr2:134918576-134918863 | Common:1; Rare:113 | ||||
| chr2:135052183-135052309 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr2:135531167-135531508 | Common:1; Rare:72 | ||||
| chr2:135741611-135741963 | Common:4; Rare:128 | ||||
| chr2:135985404-135985720 | Common:4; Rare:133; Clinvar (benign):1 | ||||
| chr2:137964085-137964515 | Common:2; Rare:70 | ||||
| chr2:138501661-138502010 | Common:2; Rare:125 | ||||
| chr2:144404867-144405262 | Common:1; Rare:85; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:144514820-144515068 | Rare:42 |