Variant report

Variant	rs13150083
Chromosome Location	chr4:30863804-30863805
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10755210	0.84[AFR][1000 genomes]
rs10939315	0.84[AFR][1000 genomes]
rs11934243	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11935059	0.82[AFR][1000 genomes]
rs11938996	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[YRI][hapmap];0.89[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11946165	0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs12503052	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13104143	0.84[EUR][1000 genomes]
rs13137577	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13144831	0.81[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs13149475	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13150968	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13152756	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1823196	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs34297806	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34410526	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35186637	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35309740	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35363488	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35509507	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs35805877	0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs35857516	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36173628	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4269140	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[YRI][hapmap];0.88[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs4293757	1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs4305479	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4352435	0.87[YRI][hapmap];0.84[AFR][1000 genomes]
rs4352436	0.84[AFR][1000 genomes]
rs4422383	0.86[YRI][hapmap];0.85[AFR][1000 genomes]
rs55982008	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56037166	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56190579	0.82[EUR][1000 genomes]
rs56338231	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60551461	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61794484	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs61794485	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs61794488	0.80[ASN][1000 genomes]
rs61795879	0.80[EUR][1000 genomes]
rs61795880	0.83[EUR][1000 genomes]
rs61795883	0.81[EUR][1000 genomes]
rs6811147	0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6811465	0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6839111	0.82[EUR][1000 genomes]
rs6842171	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6842574	0.90[JPT][hapmap];0.87[YRI][hapmap];0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6842896	0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6846615	1.00[JPT][hapmap]
rs6847898	1.00[JPT][hapmap]
rs6856866	0.89[ASN][1000 genomes]
rs6858549	0.82[AFR][1000 genomes]
rs73108238	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7674446	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7676542	1.00[JPT][hapmap]
rs958274	0.81[AMR][1000 genomes]
rs9992704	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878810	chr4:30823157-30987395	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30849200-30872200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:30855200-30879600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:30855600-30867400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:30856200-30868600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr4:30857200-30868200	Weak transcription	Aorta	Aorta
6	chr4:30859400-30864200	Weak transcription	Fetal Lung	lung
7	chr4:30859800-30864200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr4:30860600-30864800	Weak transcription	Fetal Heart	heart
9	chr4:30861800-30868000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:30862600-30867400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr4:30862800-30870600	Enhancers	Colon Smooth Muscle	Colon
12	chr4:30863000-30864600	Weak transcription	HMEC	breast
13	chr4:30863000-30868800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:30863200-30864200	Weak transcription	NHEK	skin
15	chr4:30863200-30867800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr4:30863600-30868600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:30863800-30864400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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