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PXD069116-1

PXD069116 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleMapping functional non-coding variation in individual human genomes through haplotyping, multiomics, and deep learning
DescriptionMost genetic variants in the human genome reside in non-coding regions, where they can perturb regulatory elements, influence gene expression, and contribute to various phenotypes and diseases. However, identifying such functionally relevant genetic variation remains challenging. Here we integrate personal genomics, allele-specific gene regulation, and deep learning predictions to map the impact of non-coding variation in its native allelic and regulatory context. We identify and validate hundreds of cell-type-specific transcription factor binding events disrupted by genetic variants, providing mechanistic insights underlying allele-specific gene regulation. Using this framework, we discover a rare variant that modulates PIK3R5 gene expression by disrupting an OCT2 binding site within a distal enhancer. Our study establishes a generalisable strategy for interpreting non-coding regulatory variation, enabling systematic dissection of variant effects across diverse biological systems and offering an alternative framework to investigate the disease mechanisms.
HostingRepositoryPRIDE
AnnounceDate2026-04-22
AnnouncementXMLSubmission_2026-04-22_10:20:05.691.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterMiguel Hernandez Quiles
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606;
ModificationListNo PTMs are included in the dataset
InstrumentOrbitrap Exploris 480
Dataset History
RevisionDatetimeStatusChangeLog Entry
02025-10-03 05:20:46ID requested
12026-04-22 10:20:06announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: LC-MSMS,Non-coding variants, Deep learning
Contact List
Michiel Vermeulen
contact affiliationDivision of Molecular Genetics, Oncode Institute, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands;
contact emailmi.Vermeulen@nki.nl
lab head
Miguel Hernandez Quiles
contact affiliationNetherlands Cancer Institute
contact emailm.hernandez@nki.nl
dataset submitter
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Dataset FTP location
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