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update variant and gene counts in results highlights
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README.md

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@@ -34,7 +34,7 @@ Common-variant genome-wide association studies have identified thousands of nonc
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Using 490,640 UK Biobank whole-genome sequences across 13 erythroid traits:
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- K562 FOODIE footprints show ~70-fold heritability enrichment for erythroid traits (comprising <0.5% of the genome)
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- Identified **224 common variants** and **19 rare variants** linked to TF binding sites and target genes
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- Identified **209 common variants** and **18 rare variants** linked to TF binding sites and target genes, modulating **207 unique target genes**
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- Successfully recapitulated the causal variant **rs112233623**, revealing how disruption of GATA1/TAL1 co-binding alters CCND3 regulation to drive variation in red blood cell count
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## Installation

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