Variant report

Variant	rs7537176
Chromosome Location	chr1:196311099-196311100
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10494742	0.89[CEU][hapmap];0.90[EUR][1000 genomes]
rs11806479	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs12402127	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12405050	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12407399	0.89[CEU][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12409953	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs12410633	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16839785	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56186308	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56199993	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs60040626	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61328263	0.95[AFR][1000 genomes]
rs73063982	0.85[EUR][1000 genomes]
rs73063989	0.85[EUR][1000 genomes]
rs73063993	0.85[EUR][1000 genomes]
rs73065807	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73065818	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73065825	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73065828	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73065831	0.85[AFR][1000 genomes]
rs73065844	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73067629	0.90[EUR][1000 genomes]
rs74136510	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7513135	0.89[CEU][hapmap];0.90[EUR][1000 genomes]
rs7522690	0.89[CEU][hapmap];0.90[EUR][1000 genomes]
rs7527779	0.96[YRI][hapmap];0.90[AFR][1000 genomes]
rs7554401	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832237	chr1:196205674-196328500	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv469680	chr1:196259846-196419016	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv482746	chr1:196259846-196419016	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv931415	chr1:196270759-196744780	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv872953	chr1:196286639-196411281	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv1826904	chr1:196291977-196371432	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv1009233	chr1:196301712-196568874	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
8	nsv872954	chr1:196304863-196387809	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	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	chr1:196273000-196313400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr1:196275800-196313000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr1:196279400-196314400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:196298000-196313400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:196298800-196311200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:196300200-196313600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:196301800-196313400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:196303200-196311600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr1:196303200-196312000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr1:196303200-196332600	Weak transcription	Ovary	ovary
11	chr1:196306800-196314200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:196308800-196313200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:196309200-196312000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr1:196309200-196313600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:196309200-196315600	Weak transcription	Liver	Liver
16	chr1:196310400-196311200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr1:196310600-196317400	Weak transcription	Fetal Brain Male	brain
18	chr1:196311000-196314800	Enhancers	HUES48 Cell Line	embryonic stem cell

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