| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127266791-127266902 | Common:1; Rare:39 | ||||
| chr6:127343342-127343411 | Rare:9 | ||||
| chr6:127343545-127343571 | Rare:8 | ||||
| chr6:128520569-128520781 | Common:1; Rare:79 | ||||
| chr6:131628150-131628411 | Common:2; Rare:77 | ||||
| chr6:133888958-133889142 | Common:1; Rare:30 | ||||
| chr6:135497612-135497852 | Common:4; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289774-136290020 | Common:1; Rare:106 | ||||
| chr6:137219337-137219503 | Common:3; Rare:57; Clinvar (benign):2 | ||||
| chr6:138773642-138773825 | Common:3; Rare:87 | ||||
| chr6:139028632-139028820 | Common:1; Rare:38 | ||||
| chr6:142147191-142147284 | Rare:35 | ||||
| chr6:142302393-142302654 | Common:1; Rare:56 | ||||
| chr6:143060742-143060919 | Common:7; Rare:61 | ||||
| chr6:143450667-143450921 | Common:1; Rare:97; Clinvar:4; Clinvar (benign):1 |