Variant report

Variant	rs10153833
Chromosome Location	chr2:180675114-180675115
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10930887	0.96[CEU][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13014793	1.00[JPT][hapmap]
rs13014995	0.93[CEU][hapmap]
rs1352111	0.96[CEU][hapmap];0.85[CHB][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1383413	0.83[CEU][hapmap];0.83[EUR][1000 genomes]
rs165373	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs165374	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs165379	0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs165380	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs165381	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16867014	0.81[YRI][hapmap]
rs187745	0.89[CEU][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1906012	0.92[CHB][hapmap];0.89[JPT][hapmap]
rs194674	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2170240	0.83[EUR][1000 genomes]
rs2367797	0.84[CEU][hapmap];0.84[EUR][1000 genomes]
rs259831	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs259833	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs259849	0.82[EUR][1000 genomes]
rs2630539	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28520865	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs357708	1.00[JPT][hapmap]
rs357709	1.00[JPT][hapmap]
rs357711	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs357712	0.96[CEU][hapmap];0.85[CHB][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs357714	1.00[CEU][hapmap];0.84[CHB][hapmap]
rs4894131	0.81[CEU][hapmap]
rs55869281	0.94[ASN][1000 genomes]
rs56388438	0.96[ASN][1000 genomes]
rs6725456	0.89[CEU][hapmap]
rs6752731	0.92[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7557122	0.92[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7588035	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs7597666	0.92[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7608363	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002305	chr2:180568558-180812846	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv428731	chr2:180629389-180805171	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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