Variant report

Variant	rs1808036
Chromosome Location	chr4:127542654-127542655
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:127542507..127544867-chr4:127550672..127553414,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10019530	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10027511	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10033505	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11935158	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11944598	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1511144	0.83[YRI][hapmap]
rs17011310	1.00[EUR][1000 genomes]
rs1808037	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28410886	1.00[EUR][1000 genomes]
rs28415381	0.80[AMR][1000 genomes]
rs28497310	1.00[EUR][1000 genomes]
rs28707018	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28775994	0.90[AMR][1000 genomes]
rs28783114	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28863549	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4623016	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55890724	0.90[AMR][1000 genomes]
rs6849105	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6851103	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73846055	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73846058	1.00[EUR][1000 genomes]
rs73846060	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9995088	0.90[AMR][1000 genomes]
rs9999892	0.90[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012833	chr4:127468474-127760933	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv537242	chr4:127468474-127760933	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv524850	chr4:127470903-127768849	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1013854	chr4:127508969-127663216	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1009499	chr4:127532856-127659010	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv537243	chr4:127532856-127659010	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3424263	chr4:127542609-127543344	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127541400-127548400	Weak transcription	K562	blood

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