Variant report

Variant	rs7584919
Chromosome Location	chr2:142572590-142572591
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10164495	1.00[CHB][hapmap];0.94[CHD][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs10185048	0.88[ASN][1000 genomes]
rs10496895	1.00[CHB][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10496901	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap]
rs10928122	1.00[CHB][hapmap]
rs11896904	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12104666	0.81[CHB][hapmap];0.91[JPT][hapmap];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1437339	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs1437340	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16847095	1.00[CHB][hapmap]
rs16847133	1.00[CHB][hapmap]
rs16847142	1.00[CHB][hapmap]
rs16847151	1.00[CHB][hapmap];0.94[CHD][hapmap];0.94[GIH][hapmap];0.91[JPT][hapmap]
rs16847202	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16847228	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16847265	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs16847310	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs16847314	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs16847347	0.81[CHB][hapmap]
rs16847368	0.90[CHB][hapmap]
rs16847376	0.81[CHB][hapmap]
rs1816608	1.00[CHB][hapmap]
rs1946779	1.00[CHB][hapmap];0.87[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap]
rs2164698	0.90[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs60606290	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60976197	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6721767	0.83[ASN][1000 genomes]
rs6748180	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7563727	1.00[CHB][hapmap]
rs7604400	1.00[CHB][hapmap]
rs906640	0.89[CHB][hapmap];0.91[JPT][hapmap];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs906641	1.00[CHB][hapmap];0.84[JPT][hapmap];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834394	chr2:142430225-142593264	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv530398	chr2:142474842-142843839	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875248	chr2:142527100-142572590	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
4	nsv875249	chr2:142527100-142614345	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv875250	chr2:142540240-142614345	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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