AlphaGenome variant-effect scores for rs1427407 (BCL11A erythroid enhancer, GRCh38)

AlphaGenome (Google DeepMind) variant-effect predictions for rs1427407, the lead common variant of the BCL11A erythroid enhancer, scored on GRCh38 over a 1 Mb context for both dbSNP alternate alleles (T>C and T>G) with all recommended variant scorers. The deposit contains the full scoring run (71,420 rows across 11 genomic modalities, long format, 25 columns), the stratified subset distributed with the AlphaVaR R package as example data, and the scripts that regenerate both. This is the dataset analysed in the Bioinformatics application note describing AlphaVaR; see DATASET_README.md for the full schema, per-modality track counts and checksums.