Variant report

Variant	rs2208371
Chromosome Location	chr1:171959556-171959557
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1073940	0.94[CEU][hapmap];1.00[MEX][hapmap];0.88[AMR][1000 genomes]
rs10910863	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10910881	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10910891	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12073819	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12077603	1.00[CEU][hapmap];0.93[CHB][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12090753	0.80[AMR][1000 genomes]
rs12403863	0.94[CEU][hapmap];0.94[MEX][hapmap];0.80[AMR][1000 genomes]
rs12408359	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16843679	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16843681	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2208370	0.81[JPT][hapmap];0.85[ASN][1000 genomes]
rs2224396	0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs2421950	0.88[CEU][hapmap];0.88[MEX][hapmap]
rs3736790	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.96[TSI][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55682753	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6662250	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6667114	0.94[CEU][hapmap];0.94[MEX][hapmap]
rs6668677	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6672365	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6680084	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6702539	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7525638	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7546327	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3512995	chr1:171329123-171994470	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	esv3512997	chr1:171329123-171994470	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats 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
3	nsv831893	chr1:171802450-171985000	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv532342	chr1:171922237-172133785	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 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	chr1:171949000-171976000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr1:171949400-171963600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:171952800-171962000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:171953800-171964800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr1:171953800-171967800	Weak transcription	Left Ventricle	heart
6	chr1:171954400-171968000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:171956000-171961200	Weak transcription	Adipose Nuclei	Adipose
8	chr1:171957400-171960200	Enhancers	Brain Substantia Nigra	brain
9	chr1:171958800-171960200	Enhancers	Brain Hippocampus Middle	brain
10	chr1:171958800-171966800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:171959200-171959600	Enhancers	Brain Anterior Caudate	brain
12	chr1:171959200-171960000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:171959400-171959800	Enhancers	Brain Angular Gyrus	brain
14	chr1:171959400-171960000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:171959400-171960000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr1:171959400-171960200	Enhancers	Brain Cingulate Gyrus	brain
17	chr1:171959400-171963400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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