Variant report

Variant	rs10249698
Chromosome Location	chr7:38533702-38533703
allele	A/G
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:26)

rs_ID	r²[population]
rs10229905	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10232299	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10238666	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10245053	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10247761	0.85[ASN][1000 genomes]
rs10250342	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10255786	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10259475	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10264958	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10266944	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10267691	0.96[ASN][1000 genomes]
rs10277878	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10280220	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11486852	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1158376	0.85[ASN][1000 genomes]
rs2014872	0.96[ASN][1000 genomes]
rs2267807	0.85[ASN][1000 genomes]
rs2267811	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2284248	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28412720	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2893559	0.85[ASN][1000 genomes]
rs3823595	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4419725	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4723756	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57983498	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73120255	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][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	nsv932229	chr7:38248340-38727527	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv830966	chr7:38393663-38602553	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38502600-38549400	Weak transcription	Fetal Stomach	stomach
2	chr7:38502800-38533800	Weak transcription	Aorta	Aorta
3	chr7:38524000-38543400	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr7:38524200-38545000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:38528600-38553000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:38531400-38544600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:38531800-38543800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr7:38532000-38540200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr7:38533200-38542800	Weak transcription	Fetal Muscle Trunk	muscle

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