Variant report

Variant	rs1932188
Chromosome Location	chr13:80340894-80340895
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1335287	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2027149	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2027151	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5003301	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs7139506	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7339390	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900588	chr13:80216846-80421340	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:80325000-80341400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:80338400-80341200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:80340200-80341400	Weak transcription	HMEC	breast
4	chr13:80340200-80342200	Enhancers	HUVEC	blood vessel
5	chr13:80340400-80341400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr13:80340800-80341800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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

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