| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136289329-136289459 | Rare:65 | ||||
| chr6:136289756-136290057 | Common:2; Rare:130 | ||||
| chr6:137219354-137219511 | Common:4; Rare:50; Clinvar (benign):2 | ||||
| chr6:137866922-137867233 | Rare:70 | ||||
| chr6:137867690-137867825 | Rare:23 | ||||
| chr6:138404125-138404561 | Common:7; Rare:122 | ||||
| chr6:138773646-138773825 | Common:3; Rare:85 | ||||
| chr6:139028628-139028866 | Common:1; Rare:51 | ||||
| chr6:139374644-139374788 | Common:1; Rare:49 | ||||
| chr6:142147086-142147294 | Common:3; Rare:77 | ||||
| chr6:143060752-143060919 | Common:6; Rare:60 | ||||
| chr6:143450651-143450929 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511636-143511755 | Common:3; Rare:30 | ||||
| chr6:143677730-143678068 | Common:2; Rare:80 | ||||
| chr6:143843126-143843402 | Common:2; Rare:92 |