Variant report

Variant	rs11218457
Chromosome Location	chr11:121797623-121797624
allele	C/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]
rs1079431	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10892786	0.85[EUR][1000 genomes]
rs11218458	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11218466	0.85[EUR][1000 genomes]
rs1219419	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12271581	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12281134	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12281908	0.85[EUR][1000 genomes]
rs1235044	0.85[EUR][1000 genomes]
rs1530665	0.93[ASN][1000 genomes]
rs1789735	0.85[EUR][1000 genomes]
rs3802909	0.95[ASN][1000 genomes]
rs3953235	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59708244	0.85[EUR][1000 genomes]
rs7934350	0.99[ASN][1000 genomes]
rs7939651	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121793000-121799000	Weak transcription	Fetal Kidney	kidney
2	chr11:121794800-121798400	Weak transcription	Fetal Brain Female	brain
3	chr11:121797400-121799600	Enhancers	HepG2	liver
4	chr11:121797400-121800000	Enhancers	Fetal Brain Male	brain

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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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