Variant report

Variant	rs11695923
Chromosome Location	chr2:48487207-48487208
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10195717	0.90[CEU][hapmap]
rs10495950	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11674217	0.82[CEU][hapmap]
rs11674317	0.84[EUR][1000 genomes]
rs11674475	0.89[EUR][1000 genomes]
rs11676381	0.89[EUR][1000 genomes]
rs11676925	0.90[EUR][1000 genomes]
rs11677205	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs11679518	0.83[EUR][1000 genomes]
rs11679956	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11680162	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11680657	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11680968	0.84[EUR][1000 genomes]
rs11681876	0.93[EUR][1000 genomes]
rs11683689	0.90[EUR][1000 genomes]
rs11687276	0.84[EUR][1000 genomes]
rs11687401	0.83[EUR][1000 genomes]
rs11687461	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs11687670	0.93[EUR][1000 genomes]
rs11689736	0.89[EUR][1000 genomes]
rs11691493	0.89[EUR][1000 genomes]
rs11693267	0.89[EUR][1000 genomes]
rs11889493	0.89[EUR][1000 genomes]
rs11899593	0.81[AFR][1000 genomes]
rs13398456	0.91[CEU][hapmap]
rs13431982	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17037218	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs17324965	0.90[EUR][1000 genomes]
rs17325048	0.93[EUR][1000 genomes]
rs17325209	0.99[EUR][1000 genomes]
rs17396793	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs17397094	1.00[EUR][1000 genomes]
rs17397449	0.89[CEU][hapmap]
rs2014675	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2840147	0.83[EUR][1000 genomes]
rs34135365	0.89[EUR][1000 genomes]
rs4530419	0.91[CEU][hapmap];0.89[EUR][1000 genomes]
rs55802119	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58032869	0.83[EUR][1000 genomes]
rs58136909	0.82[EUR][1000 genomes]
rs6712598	0.82[AFR][1000 genomes]
rs6713017	0.82[AFR][1000 genomes]
rs6730166	0.90[EUR][1000 genomes]
rs6733558	0.90[CEU][hapmap];0.90[EUR][1000 genomes]
rs6747738	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6759056	0.89[EUR][1000 genomes]
rs72885791	0.85[AFR][1000 genomes]
rs72885797	0.87[AFR][1000 genomes]
rs7569346	0.81[AFR][1000 genomes]
rs7571905	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7581510	0.90[EUR][1000 genomes]
rs7583719	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs952468	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009769	chr2:47972642-48509765	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv535680	chr2:47972642-48509765	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv530831	chr2:48059709-48632317	Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv519831	chr2:48072855-48566031	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv1003766	chr2:48102244-48559654	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv1005241	chr2:48413134-48493182	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv2762552	chr2:48413146-48493182	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv457407	chr2:48414735-48493182	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv581774	chr2:48414735-48493182	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1001850	chr2:48421389-48492090	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv535681	chr2:48421389-48492090	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48482000-48491400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr2:48485000-48488600	Enhancers	Placenta	Placenta
3	chr2:48486600-48492200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr2:48487000-48487400	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr2:48487200-48492000	Weak transcription	Primary monocytes fromperipheralblood	blood

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