Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:35172006-35172114 | Rare:19 | ||||
chr20:35664867-35665045 | Common:1; Rare:47 | ||||
chr20:35699305-35699481 | Rare:62; Clinvar (benign):3 | ||||
chr20:35742170-35742595 | Common:5; Rare:128 | ||||
chr20:36541325-36541551 | Common:2; Rare:70 | ||||
chr20:36573288-36573616 | Common:1; Rare:139 | ||||
chr20:36746065-36746294 | Common:2; Rare:82 | ||||
chr20:37178934-37179165 | Rare:70 | ||||
chr20:37289578-37289669 | Common:1; Rare:28 | ||||
chr20:37520919-37521266 | Common:1; Rare:83 | ||||
chr20:37524407-37524830 | Rare:73 | ||||
chr20:37527827-37528173 | Common:4; Rare:119 | ||||
chr20:38033416-38033813 | Common:2; Rare:118 | ||||
chr20:40689234-40689538 | Common:2; Rare:92 | ||||
chr20:43457802-43457925 | Rare:62 |