Variant report

Variant	rs11218431
Chromosome Location	chr11:121738368-121738369
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12273557	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61903403	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7935547	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7938656	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121735600-121740800	Weak transcription	Aorta	Aorta
2	chr11:121736600-121740600	Weak transcription	Colon Smooth Muscle	Colon
3	chr11:121737600-121738400	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr11:121737600-121738800	Enhancers	Psoas Muscle	Psoas
5	chr11:121738000-121740200	Weak transcription	Stomach Smooth Muscle	stomach

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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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