| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219316-137219479 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:137866927-137867214 | Rare:62 | ||||
| chr6:138773311-138773591 | Common:3; Rare:115 | ||||
| chr6:138773595-138773872 | Common:3; Rare:114 | ||||
| chr6:138988215-138988431 | Common:3; Rare:58 | ||||
| chr6:139028212-139028545 | Common:1; Rare:53 | ||||
| chr6:139028592-139028875 | Common:1; Rare:60 | ||||
| chr6:139029041-139029252 | Common:4; Rare:54 | ||||
| chr6:139374474-139374785 | Common:2; Rare:129 | ||||
| chr6:142147079-142147295 | Common:3; Rare:79 | ||||
| chr6:142301769-142302009 | Common:4; Rare:67 | ||||
| chr6:143060218-143060494 | Common:1; Rare:54 | ||||
| chr6:143060700-143060942 | Common:7; Rare:84 | ||||
| chr6:143164923-143165182 | Common:3; Rare:49 | ||||
| chr6:143450645-143451032 | Common:1; Rare:137; Clinvar:4; Clinvar (benign):1 |