Variant report

Variant	rs11676487
Chromosome Location	chr2:86048593-86048594
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11127000	0.94[CHB][hapmap];0.84[JPT][hapmap];0.94[ASN][1000 genomes]
rs1518986	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1518987	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs55841727	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs56075967	0.83[AFR][1000 genomes]
rs56232523	0.82[AMR][1000 genomes]
rs56363459	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs6724442	0.95[YRI][hapmap];0.94[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs6753123	0.94[YRI][hapmap];0.98[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs6756890	0.97[ASN][1000 genomes]
rs72842020	0.86[AFR][1000 genomes]
rs72842049	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7582218	0.98[ASN][1000 genomes]
rs7609014	0.88[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs7609098	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7609429	0.88[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs9677383	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs9678088	0.99[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86029800-86054400	Weak transcription	Spleen	Spleen
2	chr2:86039800-86074800	Weak transcription	Aorta	Aorta
3	chr2:86041400-86049600	Weak transcription	Lung	lung
4	chr2:86042200-86054800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:86045600-86054400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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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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