Variant report

Variant	rs11174603
Chromosome Location	chr12:40379317-40379318
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10506142	1.00[CEU][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10784340	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs10877913	0.80[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs10877955	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs10877971	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs11174831	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs11174928	0.86[JPT][hapmap]
rs11175102	0.86[JPT][hapmap]
rs11175103	0.86[JPT][hapmap]
rs12372213	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs12814744	0.94[ASN][1000 genomes]
rs12815153	0.97[ASN][1000 genomes]
rs12824918	0.82[ASN][1000 genomes]
rs17442157	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs28365683	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs28370628	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046428	chr12:40226283-40439843	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv541481	chr12:40226283-40439843	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv1052202	chr12:40322607-40406760	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40364400-40391400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:40366400-40390200	Weak transcription	Cortex derived primary cultured neurospheres	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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