Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:62551480-62551625 | Common:1; Rare:38 | ||||
chr20:63832318-63832445 | Common:1; Rare:34 | ||||
chr21:16194140-16194212 | Common:1; Rare:21 | ||||
chr21:16194238-16194616 | Common:2; Rare:107 | ||||
chr21:16211733-16212089 | Common:3; Rare:57 | ||||
chr21:25518512-25518567 | Rare:9 | ||||
chr21:28089820-28090402 | Common:10; Rare:127 | ||||
chr21:28754211-28754514 | Common:3; Rare:62 | ||||
chr21:29002654-29002811 | Common:2; Rare:52 | ||||
chr21:36320793-36320812 | Rare:8 | ||||
chr21:37536866-37537035 | Rare:33 | ||||
chr21:38760585-38760689 | Rare:22 | ||||
chr21:39788488-39788658 | Rare:38 | ||||
chr21:44549041-44549224 | Common:3; Rare:39 | ||||
chr21:45487279-45487459 | Common:3; Rare:54; Clinvar (benign):1 |