Variant report

Variant	rs11014842
Chromosome Location	chr10:26188455-26188456
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16926470	0.83[AMR][1000 genomes]
rs7085234	0.83[AMR][1000 genomes]
rs7085573	0.83[AMR][1000 genomes]
rs7896526	0.83[AMR][1000 genomes]
rs7902041	0.83[AMR][1000 genomes]
rs7924051	0.83[AMR][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	nsv894974	chr10:26028530-26322783	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1051756	chr10:26092320-26277478	Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26187200-26188600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr10:26187600-26189200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:26187800-26188600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr10:26188000-26188800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr10:26188000-26188800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr10:26188000-26189000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr10:26188200-26188800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr10:26188200-26188800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr10:26188200-26188800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr10:26188200-26188800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr10:26188200-26189000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr10:26188400-26188600	Enhancers	Primary B cells from cord blood	blood

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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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