| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133952945-133953306 | Common:2; Rare:103 | ||||
| chr6:134174731-134175034 | Common:1; Rare:155 | ||||
| chr6:134177810-134178008 | Rare:39 | ||||
| chr6:134249523-134249715 | Rare:39 | ||||
| chr6:134317849-134317998 | Rare:30 | ||||
| chr6:135054784-135054984 | Common:6; Rare:58 | ||||
| chr6:135497584-135497902 | Common:4; Rare:115; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136289767-136290054 | Common:2; Rare:124 | ||||
| chr6:136550394-136550687 | Common:2; Rare:84 | ||||
| chr6:136792509-136792659 | Common:1; Rare:51 | ||||
| chr6:136792965-136793161 | Common:1; Rare:48 | ||||
| chr6:137044689-137044755 | Rare:14 | ||||
| chr6:137219079-137219199 | Common:1; Rare:30 | ||||
| chr6:137219310-137219519 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:137866997-137867405 | Rare:92 |