Variant report

Variant	rs4457719
Chromosome Location	chr11:105709150-105709151
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10128540	0.81[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes]
rs10502062	0.81[CHB][hapmap];0.90[JPT][hapmap];0.81[MEX][hapmap];0.80[EUR][1000 genomes]
rs10502063	0.85[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes]
rs10736647	0.83[ASN][1000 genomes]
rs10750734	0.80[ASN][1000 genomes]
rs10791774	0.85[CHB][hapmap];0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs10895875	0.85[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes]
rs10895876	0.85[CHB][hapmap];0.90[JPT][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11226843	0.83[ASN][1000 genomes]
rs11226848	0.85[CHB][hapmap];0.85[JPT][hapmap];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11226849	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11226851	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1938966	0.85[CHB][hapmap];0.90[JPT][hapmap];0.81[MEX][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1938968	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1939148	0.83[ASW][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];0.81[MEX][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1954763	0.85[CHB][hapmap];0.85[JPT][hapmap];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2186598	0.83[ASW][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.81[MEX][hapmap]
rs4363555	0.85[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4636626	0.85[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs582570	0.85[CHB][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs596913	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs618301	0.85[CHB][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs621632	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs630567	0.85[CHB][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs646007	0.84[ASW][hapmap];0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.87[MKK][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs650951	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs658965	0.92[ASW][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs668120	0.83[ASW][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];0.81[MEX][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs682708	0.84[ASW][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs685424	0.83[ASW][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];0.81[MEX][hapmap];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7129691	0.80[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes]
rs748008	0.85[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7933863	0.85[CHB][hapmap];0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs7938716	0.85[CHB][hapmap];0.85[JPT][hapmap];0.83[ASN][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	nsv898357	chr11:105614894-105709856	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832257	chr11:105662753-105817576	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv1825856	chr11:105672706-105775768	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1825993	chr11:105698982-105762601	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive 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	chr11:105705200-105764600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr11:105705400-105712800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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