| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44387886-44388211 | Common:8; Rare:86 | ||||
| chr6:45377649-45377724 | Common:1; Rare:27 | ||||
| chr6:45377805-45378209 | Common:2; Rare:131 | ||||
| chr6:46129776-46130176 | Common:5; Rare:126 | ||||
| chr6:47478123-47478232 | Common:1; Rare:39; Clinvar (benign):2 | ||||
| chr6:49463141-49463453 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284670-52285132 | Common:3; Rare:145 | ||||
| chr6:52361968-52362249 | Common:4; Rare:85 | ||||
| chr6:52420089-52420386 | Common:3; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671031-52671223 | Rare:47 | ||||
| chr6:52995259-52995844 | Common:4; Rare:239 | ||||
| chr6:53061532-53061629 | Rare:18 | ||||
| chr6:53061678-53062013 | Rare:80 | ||||
| chr6:53065377-53065598 | Common:1; Rare:69 | ||||
| chr6:53348847-53349222 | Common:2; Rare:156 |