Variant report

Variant	rs57114118
Chromosome Location	chr11:85252836-85252837
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11820491	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11820534	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11821063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11821118	0.87[AMR][1000 genomes]
rs11822495	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11822876	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11822925	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11823655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11824926	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11826281	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11827119	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35243130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55684820	0.87[AMR][1000 genomes]
rs55923329	0.87[AMR][1000 genomes]
rs57770086	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58715908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59259888	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60537342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60882356	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61453055	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7928325	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7935017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7952496	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
4	nsv1050363	chr11:85163437-85293233	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv541111	chr11:85163437-85293233	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv898046	chr11:85180409-85300458	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv898047	chr11:85180409-85377707	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
9	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
10	nsv898048	chr11:85206156-85404138	Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv976462	chr11:85227017-85253774	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv898049	chr11:85231475-85292310	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv518780	chr11:85245772-85266793	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85248800-85292000	Weak transcription	Aorta	Aorta
2	chr11:85250400-85253800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr11:85250600-85253000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:85250800-85253600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:85250800-85253600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr11:85251000-85253400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr11:85251000-85253600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr11:85251000-85253800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:85251200-85253800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr11:85251200-85254000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr11:85251400-85253000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr11:85251600-85253400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr11:85251600-85259400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr11:85251600-85260200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:85251800-85253000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:85252000-85253000	Weak transcription	Brain Germinal Matrix	brain
17	chr11:85252200-85266400	Weak transcription	Ovary	ovary
18	chr11:85252600-85253400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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