Variant report

Variant	rs1366313
Chromosome Location	chr5:29888270-29888271
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10520952	0.94[CEU][hapmap]
rs10940826	0.86[EUR][1000 genomes]
rs10940827	1.00[CEU][hapmap];0.95[CHB][hapmap];0.81[YRI][hapmap]
rs11748565	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11956675	0.86[EUR][1000 genomes]
rs12523035	1.00[CEU][hapmap]
rs1428312	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1428314	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16899407	0.94[CEU][hapmap];0.95[CHB][hapmap]
rs16899413	0.83[CEU][hapmap]
rs16899416	0.83[CEU][hapmap]
rs16899419	0.83[CEU][hapmap];0.95[CHB][hapmap]
rs16899572	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16899687	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2330316	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap]
rs72745293	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs986822	0.91[AMR][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	esv3385368	chr5:29548608-29910057	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1018779	chr5:29861138-29937229	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1029641	chr5:29861138-29940871	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29887800-29889800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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