Variant report

Variant	rs10463199
Chromosome Location	chr5:96545475-96545476
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1000082	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1000083	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10068664	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10463202	1.00[CEU][hapmap]
rs10866776	0.96[ASN][1000 genomes]
rs11135499	0.89[ASN][1000 genomes]
rs12657833	0.85[EUR][1000 genomes]
rs1406325	0.96[ASN][1000 genomes]
rs1406326	0.93[ASN][1000 genomes]
rs1423499	0.85[EUR][1000 genomes]
rs1528592	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1528594	0.96[ASN][1000 genomes]
rs1609326	0.93[ASN][1000 genomes]
rs1609327	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1812918	0.82[EUR][1000 genomes]
rs1830366	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1830368	0.96[ASN][1000 genomes]
rs183410	0.89[ASN][1000 genomes]
rs1852739	0.93[ASN][1000 genomes]
rs1862592	0.96[ASN][1000 genomes]
rs1919244	0.96[ASN][1000 genomes]
rs1919245	0.96[ASN][1000 genomes]
rs1997296	0.96[ASN][1000 genomes]
rs2081139	0.96[ASN][1000 genomes]
rs2081140	0.96[ASN][1000 genomes]
rs2081142	0.96[ASN][1000 genomes]
rs2098708	0.85[EUR][1000 genomes]
rs2113018	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs2161571	0.85[EUR][1000 genomes]
rs2351504	0.89[ASN][1000 genomes]
rs2351505	0.82[EUR][1000 genomes]
rs2351506	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2548412	0.82[JPT][hapmap]
rs2548423	0.96[ASN][1000 genomes]
rs2643465	0.93[ASN][1000 genomes]
rs2643496	0.93[ASN][1000 genomes]
rs2643503	0.93[ASN][1000 genomes]
rs2643577	0.93[ASN][1000 genomes]
rs2697598	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2697637	0.93[ASN][1000 genomes]
rs3108540	0.89[ASN][1000 genomes]
rs317110	0.85[EUR][1000 genomes]
rs317112	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs36139969	0.81[EUR][1000 genomes]
rs4626360	0.85[EUR][1000 genomes]
rs4869152	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4869153	0.96[ASN][1000 genomes]
rs4869156	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs56773447	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6556953	0.93[ASN][1000 genomes]
rs6874040	0.96[ASN][1000 genomes]
rs6899065	0.96[ASN][1000 genomes]
rs7723203	0.96[ASN][1000 genomes]
rs9314193	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9686259	0.96[ASN][1000 genomes]
rs9687077	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs972717	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv830412	chr5:96427305-96606619	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers 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	18 gene(s)	inside rSNPs	diseases
4	nsv1019790	chr5:96471680-96980633	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv537812	chr5:96471680-96980633	ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Weak transcription 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	24 gene(s)	inside rSNPs	diseases
6	nsv882392	chr5:96496189-96546238	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv882393	chr5:96496189-96567950	Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv534326	chr5:96531217-97283481	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv882394	chr5:96538585-97108559	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96545000-96545600	Enhancers	Dnd41	blood

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