| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:135054731-135054962 | Common:6; Rare:74 | ||||
| chr6:135497585-135497873 | Common:4; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136289747-136290032 | Common:1; Rare:124 | ||||
| chr6:137219330-137219493 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr6:137866922-137867389 | Rare:105 | ||||
| chr6:138107127-138107155 | Rare:8 | ||||
| chr6:138404150-138404569 | Common:7; Rare:113 | ||||
| chr6:138773543-138773894 | Common:3; Rare:144 | ||||
| chr6:139374411-139374799 | Common:4; Rare:155 | ||||
| chr6:142147140-142147304 | Rare:67 | ||||
| chr6:143060724-143060928 | Common:7; Rare:72 | ||||
| chr6:143450642-143450961 | Common:1; Rare:118; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511651-143511817 | Common:4; Rare:39 | ||||
| chr6:143843179-143843409 | Common:2; Rare:74 | ||||
| chr6:144150411-144150521 | Common:2; Rare:32 |