| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:133568255-133568354 | Rare:18 | ||||
| chr2:134838175-134838684 | Common:4; Rare:110 | ||||
| chr2:134918702-134918863 | Rare:64 | ||||
| chr2:135531172-135531521 | Common:1; Rare:74 | ||||
| chr2:135985404-135985685 | Common:4; Rare:125; Clinvar (benign):1 | ||||
| chr2:137964085-137964622 | Common:2; Rare:99 | ||||
| chr2:138501645-138502017 | Common:4; Rare:139 | ||||
| chr2:142877508-142877732 | Common:2; Rare:36 | ||||
| chr2:144332453-144332753 | Common:1; Rare:118 | ||||
| chr2:144517328-144517636 | Common:5; Rare:85; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:148020673-148021096 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:149587087-149587456 | Common:4; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:149587674-149587852 | Common:1; Rare:49; Clinvar:1 | ||||
| chr2:150487092-150487272 | Common:6; Rare:40 | ||||
| chr2:151289602-151289704 | Common:1; Rare:28 |