Variant report

Variant	rs11233682
Chromosome Location	chr11:83291850-83291851
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10792690	0.82[ASN][1000 genomes]
rs493431	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs494303	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs515618	0.92[ASN][1000 genomes]
rs532467	0.82[ASN][1000 genomes]
rs535755	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs543147	0.80[ASN][1000 genomes]
rs548327	0.81[EUR][1000 genomes]
rs558211	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs560846	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs561890	0.85[ASN][1000 genomes]
rs591422	0.81[ASN][1000 genomes]
rs653546	0.80[ASN][1000 genomes]
rs684110	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83286400-83294200	Weak transcription	NHEK	skin
2	chr11:83290200-83294200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:83290400-83294200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	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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