Variant report

Variant	rs529651677
Chromosome Location	chr13:88537150-88537151
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832673	chr13:88431110-88607319	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv562632	chr13:88532287-88622740	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:88536800-88537800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr13:88537000-88537200	Active TSS	Brain Hippocampus Middle	brain
3	chr13:88537000-88537400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr13:88537000-88537400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:88537000-88537400	Enhancers	Brain Cingulate Gyrus	brain
6	chr13:88537000-88537400	Enhancers	Fetal Heart	heart
7	chr13:88537000-88537600	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr13:88537000-88538200	Enhancers	Cortex derived primary cultured neurospheres	brain

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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