Variant report

Variant rs35778743
Chromosome Location chr2:212589986-212589987
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:212569400-212590800 Weak transcription Fetal Kidney kidney
2 chr2:212569600-212591800 Weak transcription Fetal Heart heart
3 chr2:212571200-212594800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:212575600-212592000 Weak transcription Aorta Aorta
5 chr2:212583600-212595400 Weak transcription Brain Anterior Caudate brain
6 chr2:212586200-212590800 Weak transcription Brain Hippocampus Middle brain
7 chr2:212587400-212595000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr2:212589600-212590000 Flanking Active TSS Brain Substantia Nigra brain
9 chr2:212589800-212590000 Enhancers Brain Angular Gyrus brain
10 chr2:212589800-212590000 Enhancers Left Ventricle heart
11 chr2:212589800-212590400 Enhancers Brain Inferior Temporal Lobe brain

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