Functional noncoding variants within TBX1 enhancer contribute to Tetralogy of Fallot

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Authors: Jimiao Gao
Cited by: 0

Abstract

This dataset contains single-cell RNA-sequencing (scRNA-seq) and chromatin immunoprecipitation sequencing (ChIP-seq) data generated from human embryonic stem cell (hESC)–derived vascular organoids. Vascular organoids were differentiated from wild-type (WT) and TBX1 enhancer-deleted hESC lines and collected at four developmental stages (Day 0, Day 5, Day 10, and Day 15) to model early human vascular lineage specification and maturation in vitro.

Fields of Study & Subjects

Congenital heart defects research Congenital Heart Disease Studies Cardiac electrophysiology and arrhythmias

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
10 February 2026
Language
EN
Document type
Dataset