Variant report

Variant	rs9495641
Chromosome Location	chr6:140451403-140451404
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs13204837	0.88[YRI][hapmap]
rs1416289	0.88[YRI][hapmap]
rs592056	0.88[YRI][hapmap]
rs60402795	0.88[AFR][1000 genomes]
rs618515	0.90[YRI][hapmap]
rs647968	0.90[YRI][hapmap]
rs6931550	1.00[AMR][1000 genomes]
rs6931710	1.00[AMR][1000 genomes]
rs724061	0.90[YRI][hapmap]
rs7774706	0.82[YRI][hapmap]
rs9399298	0.90[YRI][hapmap]
rs9403134	0.90[YRI][hapmap]
rs9495636	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9495644	0.88[AFR][1000 genomes]
rs9495648	0.82[YRI][hapmap];0.83[AFR][1000 genomes]
rs9495651	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869066	chr6:139777114-140639695	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv1016532	chr6:140174639-141029988	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
3	nsv1022987	chr6:140344229-140463916	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv886693	chr6:140444057-140578494	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140444000-140460800	Weak transcription	K562	blood
2	chr6:140448200-140453600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:140450400-140457400	Weak transcription	Placenta	Placenta
4	chr6:140450400-140459600	Weak transcription	Pancreas	Pancrea
5	chr6:140451200-140451600	ZNF genes & repeats	Liver	Liver

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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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