Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:47314114-47314461 | Common:3; Rare:71 | ||||
chr1:47333681-47333972 | Common:3; Rare:92 | ||||
chr1:48776725-48776780 | Rare:15 | ||||
chr1:50960222-50960398 | Rare:48 | ||||
chr1:50970097-50970257 | Rare:31 | ||||
chr1:52055158-52055339 | Common:1; Rare:48 | ||||
chr1:52056070-52056350 | Common:2; Rare:76 | ||||
chr1:52404467-52404626 | Common:1; Rare:47 | ||||
chr1:52553069-52553384 | Common:4; Rare:88 | ||||
chr1:53220340-53220666 | Common:2; Rare:145 | ||||
chr1:53238460-53238592 | Rare:59 | ||||
chr1:53946253-53946494 | Common:1; Rare:87 | ||||
chr1:54053184-54053654 | Common:6; Rare:158 | ||||
chr1:54200017-54200213 | Rare:46 | ||||
chr1:58577249-58577493 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 |