Variant report

Variant	rs4756025
Chromosome Location	chr11:33825832-33825833
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11032380	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11032413	0.80[AMR][1000 genomes]
rs11032417	0.83[EUR][1000 genomes]
rs12282096	1.00[CEU][hapmap]
rs12361553	1.00[CEU][hapmap]
rs12420267	0.88[CEU][hapmap];0.84[AMR][1000 genomes]
rs12797549	0.84[AMR][1000 genomes]
rs2056396	1.00[CEU][hapmap]
rs4755340	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756031	0.82[EUR][1000 genomes]
rs4756052	0.82[AMR][1000 genomes]
rs66951942	0.84[EUR][1000 genomes]
rs7125621	1.00[CEU][hapmap]
rs7927218	0.94[CEU][hapmap]
rs939804	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs953871	0.82[CEU][hapmap]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33824600-33830000	Weak transcription	Fetal Brain Male	brain
2	chr11:33825200-33827000	Bivalent Enhancer	Fetal Lung	lung

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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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