Variant report

Variant	rs13103597
Chromosome Location	chr4:143558581-143558582
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10000770	0.94[AMR][1000 genomes]
rs10006418	0.94[AMR][1000 genomes]
rs10015404	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs10020322	0.86[AMR][1000 genomes]
rs10020865	0.94[AMR][1000 genomes]
rs11732693	0.81[AMR][1000 genomes]
rs13114437	0.89[AMR][1000 genomes]
rs13353799	0.94[AMR][1000 genomes]
rs1348362	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs1348363	0.94[AMR][1000 genomes]
rs28415364	0.94[AMR][1000 genomes]
rs28485272	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs28673920	0.94[AMR][1000 genomes]
rs28733118	0.89[AMR][1000 genomes]
rs28758601	0.86[AMR][1000 genomes]
rs34082059	0.94[AMR][1000 genomes]
rs34234953	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs34393544	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs35255414	0.86[AMR][1000 genomes]
rs35366693	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs36101393	0.94[AMR][1000 genomes]
rs36142547	0.81[AMR][1000 genomes]
rs60361448	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs62330251	0.86[AMR][1000 genomes]
rs62331862	0.89[AMR][1000 genomes]
rs6834451	0.89[AMR][1000 genomes]
rs6849164	0.94[AMR][1000 genomes]
rs6856817	0.86[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	nsv830101	chr4:143518810-143684392	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143537000-143575800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:143556000-143559400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:143558400-143558800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
4	chr4:143558400-143559200	ZNF genes & repeats	Primary hematopoietic stem cells	blood

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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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