Variant report

Variant	rs6774032
Chromosome Location	chr3:143419181-143419182
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12629688	0.82[JPT][hapmap]
rs13059265	0.87[CEU][hapmap];0.81[JPT][hapmap];0.80[EUR][1000 genomes]
rs1345170	0.91[JPT][hapmap]
rs16853999	0.83[JPT][hapmap]
rs1868174	0.83[JPT][hapmap]
rs1868175	0.87[CEU][hapmap]
rs4839649	0.83[JPT][hapmap]
rs4839650	0.81[CHB][hapmap]
rs6774050	0.84[CEU][hapmap];1.00[CHB][hapmap];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6786893	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6786896	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs935519	0.87[CEU][hapmap];0.88[GIH][hapmap];0.95[TSI][hapmap]
rs935520	0.86[CEU][hapmap];0.82[JPT][hapmap]

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	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv877566	chr3:143397740-143421221	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143370800-143420800	Weak transcription	Primary T cells from cord blood	blood
2	chr3:143394200-143470200	Weak transcription	Primary B cells from cord blood	blood
3	chr3:143416800-143419200	Enhancers	Brain Anterior Caudate	brain
4	chr3:143417200-143419400	Enhancers	Brain Hippocampus Middle	brain
5	chr3:143417600-143419400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
6	chr3:143418000-143431200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:143418600-143419400	Enhancers	Spleen	Spleen
8	chr3:143418800-143426600	Weak transcription	Fetal Lung	lung
9	chr3:143418800-143428600	Weak transcription	Brain Angular Gyrus	brain
10	chr3:143419000-143419200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr3:143419000-143426800	Weak transcription	Psoas Muscle	Psoas

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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