Variant report

Variant	rs2707374
Chromosome Location	chr7:106723926-106723927
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10249401	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2299419	0.87[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2536503	1.00[ASN][1000 genomes]
rs2536505	1.00[ASN][1000 genomes]
rs2707373	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28362525	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59103028	0.89[EUR][1000 genomes]
rs6466156	0.93[YRI][hapmap];0.86[AFR][1000 genomes]
rs73413360	0.85[EUR][1000 genomes]
rs73413372	0.87[EUR][1000 genomes]
rs9656135	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831087	chr7:106673465-106872460	Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv608072	chr7:106718347-106753248	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv32754	chr7:106723808-106728719	Weak transcription Enhancers ZNF genes & repeats	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	chr7:106718000-106730600	Weak transcription	Fetal Brain Female	brain
2	chr7:106718800-106727800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:106719400-106730400	Weak transcription	Fetal Brain Male	brain
4	chr7:106719400-106734200	Weak transcription	Brain Anterior Caudate	brain
5	chr7:106719800-106730600	Weak transcription	Brain Germinal Matrix	brain
6	chr7:106720200-106727000	Weak transcription	Pancreas	Pancrea
7	chr7:106720800-106730600	Weak transcription	Lung	lung
8	chr7:106720800-106730800	Weak transcription	Fetal Stomach	stomach
9	chr7:106721000-106730200	Weak transcription	Fetal Heart	heart
10	chr7:106721800-106730600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr7:106722600-106727800	Weak transcription	K562	blood

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

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