Variant report

Variant	rs10945951
Chromosome Location	chr6:164503129-164503130
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10455794	0.83[ASN][1000 genomes]
rs10755598	0.83[ASN][1000 genomes]
rs10806788	0.83[ASN][1000 genomes]
rs10806789	0.83[ASN][1000 genomes]
rs10945948	0.88[ASN][1000 genomes]
rs10945949	0.83[ASN][1000 genomes]
rs10945950	0.83[ASN][1000 genomes]
rs12055516	0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12055870	0.81[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12175904	0.80[ASN][1000 genomes]
rs12200189	0.82[ASN][1000 genomes]
rs12204824	0.80[ASN][1000 genomes]
rs12208775	0.82[ASN][1000 genomes]
rs12208802	0.82[ASN][1000 genomes]
rs12216473	0.82[ASN][1000 genomes]
rs12216523	0.80[ASN][1000 genomes]
rs12527246	0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12527249	0.85[ASN][1000 genomes]
rs12530262	0.83[ASN][1000 genomes]
rs13212664	0.83[ASN][1000 genomes]
rs1436856	0.83[ASN][1000 genomes]
rs1436857	0.83[ASN][1000 genomes]
rs1436858	0.83[ASN][1000 genomes]
rs1436859	0.83[ASN][1000 genomes]
rs1436860	0.83[ASN][1000 genomes]
rs1898308	0.82[ASN][1000 genomes]
rs2033705	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs206688	0.80[ASN][1000 genomes]
rs34312142	0.80[ASN][1000 genomes]
rs35317099	0.83[ASN][1000 genomes]
rs366572	0.80[ASN][1000 genomes]
rs369635	0.80[ASN][1000 genomes]
rs377662	0.80[ASN][1000 genomes]
rs379046	0.80[ASN][1000 genomes]
rs379084	0.80[ASN][1000 genomes]
rs380640	0.80[ASN][1000 genomes]
rs383861	0.80[ASN][1000 genomes]
rs384090	0.80[ASN][1000 genomes]
rs386112	0.80[ASN][1000 genomes]
rs390097	0.80[ASN][1000 genomes]
rs390662	0.80[ASN][1000 genomes]
rs392649	0.80[ASN][1000 genomes]
rs411505	0.80[ASN][1000 genomes]
rs412544	0.80[ASN][1000 genomes]
rs412553	0.80[ASN][1000 genomes]
rs414708	0.80[ASN][1000 genomes]
rs418309	0.80[ASN][1000 genomes]
rs418319	0.80[ASN][1000 genomes]
rs419927	0.80[ASN][1000 genomes]
rs422371	0.80[ASN][1000 genomes]
rs422805	0.80[ASN][1000 genomes]
rs429361	0.80[ASN][1000 genomes]
rs71569438	0.85[ASN][1000 genomes]
rs71569439	0.85[ASN][1000 genomes]
rs9346989	0.80[ASN][1000 genomes]
rs9346990	0.80[ASN][1000 genomes]
rs9346991	0.82[ASN][1000 genomes]
rs9347816	0.80[ASN][1000 genomes]
rs9347817	0.82[ASN][1000 genomes]
rs9355459	0.83[ASN][1000 genomes]
rs9364714	0.89[ASN][1000 genomes]
rs9364715	0.80[ASN][1000 genomes]
rs9365656	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1029952	chr6:164463355-165268911	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164492600-164504800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:164499200-164505200	Weak transcription	Right Ventricle	heart
3	chr6:164499400-164503800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:164499400-164505400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:164499600-164506000	Weak transcription	HSMMtube	muscle
6	chr6:164499800-164503400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:164500000-164505200	Weak transcription	Brain Anterior Caudate	brain
8	chr6:164500400-164505200	Weak transcription	Right Atrium	heart
9	chr6:164501400-164503400	Enhancers	Fetal Muscle Trunk	muscle
10	chr6:164501400-164506800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr6:164501600-164503400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr6:164501800-164505000	Weak transcription	Spleen	Spleen
13	chr6:164502200-164503200	Enhancers	Fetal Muscle Leg	muscle
14	chr6:164502400-164505000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr6:164502400-164505200	Weak transcription	Fetal Heart	heart
16	chr6:164502600-164506200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:164502800-164503400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:164502800-164503400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr6:164503000-164503200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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