| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:131628205-131628491 | Common:2; Rare:69 | ||||
| chr6:131951369-131951404 | Rare:12 | ||||
| chr6:132513052-132513246 | Common:1; Rare:47 | ||||
| chr6:132814272-132814611 | Common:4; Rare:122 | ||||
| chr6:133952948-133953227 | Common:2; Rare:72 | ||||
| chr6:134174841-134175052 | Common:1; Rare:107 | ||||
| chr6:135497612-135497863 | Common:4; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289774-136290032 | Common:1; Rare:112 | ||||
| chr6:137219356-137219458 | Common:2; Rare:34; Clinvar (benign):2 | ||||
| chr6:138773646-138773836 | Common:3; Rare:88 | ||||
| chr6:142147179-142147279 | Rare:36 | ||||
| chr6:143060742-143060919 | Common:7; Rare:61 | ||||
| chr6:143450667-143450884 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:144285153-144285335 | Common:2; Rare:57 | ||||
| chr6:151391537-151391835 | Common:3; Rare:76 |