Variant report

Variant	rs2661715
Chromosome Location	chr12:75007480-75007481
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1157081	0.86[ASN][1000 genomes]
rs11832914	0.98[EUR][1000 genomes]
rs11836744	0.98[EUR][1000 genomes]
rs12814597	0.98[EUR][1000 genomes]
rs12816124	0.98[EUR][1000 genomes]
rs12818780	0.97[EUR][1000 genomes]
rs12832355	0.98[EUR][1000 genomes]
rs1493813	0.83[CEU][hapmap];0.86[ASN][1000 genomes]
rs1493820	0.98[EUR][1000 genomes]
rs17113865	0.92[EUR][1000 genomes]
rs17113909	0.97[EUR][1000 genomes]
rs17113938	0.98[EUR][1000 genomes]
rs1972018	0.98[EUR][1000 genomes]
rs1994886	0.86[ASN][1000 genomes]
rs2131714	0.86[ASN][1000 genomes]
rs2131715	0.86[ASN][1000 genomes]
rs2131716	0.86[ASN][1000 genomes]
rs2172600	0.86[ASN][1000 genomes]
rs2605349	0.83[CEU][hapmap]
rs2605353	0.86[ASN][1000 genomes]
rs2605354	0.86[ASN][1000 genomes]
rs2605356	0.86[ASN][1000 genomes]
rs2605357	0.86[ASN][1000 genomes]
rs2605359	0.86[ASN][1000 genomes]
rs2641455	0.81[CEU][hapmap];0.86[ASN][1000 genomes]
rs2641456	0.83[CEU][hapmap]
rs2661709	0.86[ASN][1000 genomes]
rs2661710	0.83[CEU][hapmap];0.86[ASN][1000 genomes]
rs2661716	0.86[ASN][1000 genomes]
rs3905797	0.98[EUR][1000 genomes]
rs3905798	0.98[EUR][1000 genomes]
rs59679678	0.98[EUR][1000 genomes]
rs71458192	0.98[EUR][1000 genomes]
rs7976081	0.97[EUR][1000 genomes]
rs903167	0.86[ASN][1000 genomes]
rs903168	0.86[ASN][1000 genomes]
rs996431	0.83[CEU][hapmap];0.86[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	esv3325789	chr12:75006185-75011483	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:75007400-75008000	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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