Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:127343331-127343639 | Common:2; Rare:72 | ||||
chr6:128520575-128520718 | Rare:52 | ||||
chr6:131628101-131628471 | Common:3; Rare:96 | ||||
chr6:132401478-132401584 | Common:1; Rare:32 | ||||
chr6:132814304-132814617 | Common:3; Rare:120 | ||||
chr6:134177833-134178091 | Common:1; Rare:42 | ||||
chr6:136289779-136290037 | Common:1; Rare:112 | ||||
chr6:137866941-137867237 | Rare:66 | ||||
chr6:138107473-138107770 | Common:5; Rare:66 | ||||
chr6:138572457-138572723 | Common:2; Rare:56 | ||||
chr6:138773669-138773813 | Common:3; Rare:70 | ||||
chr6:142301874-142302077 | Common:3; Rare:59 | ||||
chr6:143450651-143450965 | Common:1; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
chr6:144285130-144285347 | Common:2; Rare:72 | ||||
chr6:144285544-144285781 | Common:3; Rare:57 |