Variant report

Variant	rs10195937
Chromosome Location	chr2:76997763-76997764
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10188955	0.87[CEU][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12612861	1.00[CEU][hapmap];0.87[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12620459	1.00[ASW][hapmap];1.00[CEU][hapmap];0.87[JPT][hapmap];0.88[LWK][hapmap];0.87[MEX][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12713883	0.88[CEU][hapmap];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12995505	1.00[MEX][hapmap];0.98[AMR][1000 genomes]
rs13008894	0.88[CEU][hapmap];1.00[MEX][hapmap];0.96[AMR][1000 genomes]
rs13030721	0.88[CEU][hapmap];1.00[MEX][hapmap];0.87[AMR][1000 genomes]
rs13398294	1.00[YRI][hapmap]
rs13400865	1.00[YRI][hapmap]
rs13405269	1.00[YRI][hapmap]
rs1517783	1.00[CEU][hapmap];0.87[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1914507	0.87[CEU][hapmap];0.87[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56961208	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59960669	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs60881718	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6718624	0.88[CEU][hapmap];1.00[MEX][hapmap];0.96[AMR][1000 genomes]
rs7560515	0.88[CEU][hapmap];0.93[MEX][hapmap];0.96[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv582235	chr2:76881210-76997763	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv874320	chr2:76971709-77013724	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
3	nsv1011401	chr2:76982546-77068714	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv999822	chr2:76994539-77022762	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region	1 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	chr2:76988000-76998400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:76994600-76998000	Weak transcription	hESC Derived CD184+ Endoderm 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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