Variant report

Variant	rs10496911
Chromosome Location	chr2:142783437-142783438
allele	A/G
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]
rs10496910	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12617190	0.95[GIH][hapmap]
rs12617257	1.00[GIH][hapmap]
rs12617281	1.00[GIH][hapmap]
rs12617322	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs12617486	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12620001	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12623699	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12623786	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs13394203	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16847932	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16847936	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16847942	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6739226	1.00[ASN][1000 genomes]
rs7559509	1.00[CEU][hapmap]
rs965765	0.85[CHB][hapmap]

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	nsv530398	chr2:142474842-142843839	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv997274	chr2:142760393-143599193	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv526107	chr2:142768518-142884248	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142782800-142783600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:142783000-142783600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr2:142783000-142783800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:142783000-142783800	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr2:142783200-142783600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr2:142783400-142783800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:142783400-142784000	Enhancers	H1 BMP4 Derived Mesendoderm 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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