Variant report

Variant	rs3778359
Chromosome Location	chr6:6150382-6150383
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1871970	0.90[CHB][hapmap];0.91[CHD][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs2326705	0.90[CHB][hapmap];0.88[CHD][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs2326708	0.90[CHB][hapmap];0.88[CHD][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs3024454	0.90[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs900402	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap];1.00[ASN][1000 genomes]
rs9379013	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.96[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9392751	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];0.95[TSI][hapmap];0.88[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9392752	1.00[CEU][hapmap];0.85[CHD][hapmap];0.96[GIH][hapmap];0.92[JPT][hapmap];0.91[TSI][hapmap];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9504695	0.93[JPT][hapmap]

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	nsv1031283	chr6:6084559-6160039	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:6144000-6163600	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr6:6144200-6151600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr6:6145000-6179800	Weak transcription	HSMM	muscle
4	chr6:6146800-6160200	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr6:6146800-6200400	Weak transcription	Placenta	Placenta
6	chr6:6148400-6156200	Strong transcription	HSMMtube	muscle
7	chr6:6149400-6151400	Weak transcription	Liver	Liver
8	chr6:6150200-6151800	Weak transcription	Adipose Nuclei	Adipose

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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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