| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125780998-125781138 | Rare:25 | ||||
| chr6:125956661-125956781 | Common:1; Rare:41 | ||||
| chr6:125986401-125986548 | Rare:53 | ||||
| chr6:127343347-127343411 | Rare:8 | ||||
| chr6:128520564-128520798 | Common:1; Rare:87 | ||||
| chr6:133953092-133953227 | Common:2; Rare:39 | ||||
| chr6:135497649-135497901 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289773-136289951 | Common:1; Rare:72 | ||||
| chr6:136550396-136550687 | Common:2; Rare:83 | ||||
| chr6:137219341-137219493 | Common:2; Rare:50; Clinvar (benign):2 | ||||
| chr6:138773730-138773795 | Common:1; Rare:36 | ||||
| chr6:139028606-139028820 | Common:1; Rare:44 | ||||
| chr6:143060733-143060919 | Common:7; Rare:64 | ||||
| chr6:143450669-143450884 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:149546010-149546159 | Rare:63 |