Variant report

Variant	rs59006629
Chromosome Location	chr11:127471100-127471101
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1367796	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2060093	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2060094	1.00[AMR][1000 genomes]
rs7114318	1.00[AMR][1000 genomes]
rs7928375	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7928874	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036740	chr11:126625228-127528450	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
2	nsv898445	chr11:127377733-127713173	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1043894	chr11:127423435-127637119	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv541202	chr11:127423435-127637119	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:127470400-127472000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:127470600-127471400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr11:127470800-127471400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:127470800-127472000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:127471000-127471400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr11:127471000-127471800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr11:127471000-127472200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr11:127471000-127472800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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