Variant report

Variant	rs11186679
Chromosome Location	chr10:93522131-93522132
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:15)

rs_ID	r²[population]
rs1028934	1.00[ASN][1000 genomes]
rs10881982	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs11186619	1.00[ASN][1000 genomes]
rs11186638	1.00[ASN][1000 genomes]
rs11186641	1.00[ASN][1000 genomes]
rs11186661	1.00[ASN][1000 genomes]
rs11186698	0.90[EUR][1000 genomes]
rs11186708	0.81[EUR][1000 genomes]
rs11186716	0.81[EUR][1000 genomes]
rs3802649	0.90[EUR][1000 genomes]
rs4382814	1.00[ASN][1000 genomes]
rs60854684	1.00[ASN][1000 genomes]
rs61874526	1.00[ASN][1000 genomes]
rs61874527	1.00[ASN][1000 genomes]
rs61874529	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv975785	chr10:93501141-93525212	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93521600-93522400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr10:93522000-93522200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:93522000-93522200	Enhancers	Monocytes-CD14+_RO01746	blood

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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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