Update README.md

README.md

@@ -60,7 +60,7 @@ Single Nucleotide Variants (SNVs) as Pathogenic or Benign using structured genom
 
 - Base model: unsloth/qwen3-4b-instruct-2507-unsloth-bnb-4bit
 - Fine-tuning: LoRA via Unsloth
-- Training data: 1.2 million SNVs
+- **Training data: 1.2 million SNVs**
 - Genome assembly: GRCh38
 - Scope: SNVs only
 - Deployment: safetensors + GGUF (Q4/Q8)