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Rare penetrant mutations confer severe risk of common diseases
UploadA cross-disorder dosage sensitivity map of the human genome
UploadGenome-wide enhancer maps link risk variants to disease genes
UploadControl of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation
UploadInterrogation of human hematopoiesis at single-cell and single-variant resolution
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