Variant report

Variant	rs12264704
Chromosome Location	chr10:28111039-28111040
allele	G/T
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]
rs10159551	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11006730	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12245082	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12249609	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2065689	1.00[CEU][hapmap]
rs58550563	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7077784	1.00[CEU][hapmap]
rs73604076	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73604077	0.85[EUR][1000 genomes]
rs73604079	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs952403	0.92[AMR][1000 genomes];1.00[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	nsv831813	chr10:28017606-28200651	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv971859	chr10:28070066-28271252	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28105600-28127600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr10:28109400-28111200	Weak transcription	Fetal Stomach	stomach
3	chr10:28109400-28111200	Weak transcription	Ovary	ovary
4	chr10:28110000-28111400	Weak transcription	Left Ventricle	heart
5	chr10:28110000-28111600	Weak transcription	Aorta	Aorta
6	chr10:28110000-28113200	Weak transcription	Pancreas	Pancrea
7	chr10:28110200-28111600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr10:28111000-28111200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:28111000-28111400	Enhancers	Colon Smooth Muscle	Colon
10	chr10:28111000-28111600	Enhancers	Rectal Smooth Muscle	rectum

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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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