Variant report

Variant	rs10261812
Chromosome Location	chr7:103370579-103370580
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10229702	0.82[EUR][1000 genomes]
rs10234931	0.82[EUR][1000 genomes]
rs10235072	0.82[EUR][1000 genomes]
rs10242211	0.82[EUR][1000 genomes]
rs10257295	0.82[EUR][1000 genomes]
rs10265623	0.82[EUR][1000 genomes]
rs10480649	0.82[EUR][1000 genomes]
rs11974290	0.82[EUR][1000 genomes]
rs11976904	0.82[EUR][1000 genomes]
rs3025969	0.82[EUR][1000 genomes]
rs56255035	0.82[EUR][1000 genomes]
rs6977938	0.82[EUR][1000 genomes]
rs73410852	0.82[EUR][1000 genomes]
rs73410854	0.82[EUR][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	nsv491911	chr7:102967150-103403622	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv427799	chr7:103250733-103454202	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103355400-103374800	Weak transcription	HepG2	liver
2	chr7:103370400-103371400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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