Variant report

Variant	rs6886264
Chromosome Location	chr5:29798201-29798202
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10940817	0.83[AMR][1000 genomes]
rs11737948	0.84[AMR][1000 genomes]
rs11745229	0.84[AMR][1000 genomes]
rs11745291	0.83[AMR][1000 genomes]
rs11954752	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12516688	0.86[AMR][1000 genomes]
rs12517227	0.86[AMR][1000 genomes]
rs12517273	0.86[AMR][1000 genomes]
rs12651890	0.84[AMR][1000 genomes]
rs12651934	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12656086	0.81[AMR][1000 genomes]
rs1350222	0.84[AMR][1000 genomes]
rs1456641	0.86[AMR][1000 genomes]
rs1456642	0.86[AMR][1000 genomes]
rs1456643	0.87[AMR][1000 genomes]
rs1563510	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs16899413	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16899416	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16899422	0.84[AMR][1000 genomes]
rs2219325	0.84[AMR][1000 genomes]
rs2330137	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2330138	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2330139	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2925526	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2972789	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs58306893	0.83[AMR][1000 genomes]
rs58977762	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59897238	0.81[AMR][1000 genomes]
rs61330469	0.80[AMR][1000 genomes]
rs61531233	0.84[AMR][1000 genomes]
rs66702955	0.84[AMR][1000 genomes]
rs6877378	0.86[AMR][1000 genomes]
rs6893901	0.85[ASN][1000 genomes]
rs72743275	0.81[AMR][1000 genomes]
rs9292341	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];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	nsv1016603	chr5:29102713-29843965	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv537712	chr5:29102713-29843965	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	esv3385368	chr5:29548608-29910057	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1029329	chr5:29778216-29805002	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1026460	chr5:29785485-29814309	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
6	nsv1034228	chr5:29785485-29815868	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
7	nsv1018046	chr5:29785776-29818396	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
8	nsv1019541	chr5:29786932-29814309	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
9	nsv1016811	chr5:29786932-29824596	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29796400-29801000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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