Variant report

Variant	rs60739746
Chromosome Location	chr3:161293589-161293590
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs13325090	1.00[EUR][1000 genomes]
rs16832385	1.00[EUR][1000 genomes]
rs16833201	1.00[EUR][1000 genomes]
rs2404345	1.00[EUR][1000 genomes]
rs28559591	1.00[EUR][1000 genomes]
rs57175632	1.00[EUR][1000 genomes]
rs59860665	1.00[EUR][1000 genomes]
rs59865680	1.00[EUR][1000 genomes]
rs60125032	1.00[EUR][1000 genomes]
rs60172527	1.00[EUR][1000 genomes]
rs60680460	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6780511	1.00[EUR][1000 genomes]
rs73021435	1.00[EUR][1000 genomes]
rs73875623	1.00[EUR][1000 genomes]
rs73877461	1.00[EUR][1000 genomes]
rs73878333	1.00[EUR][1000 genomes]
rs73878336	1.00[EUR][1000 genomes]
rs9820241	1.00[EUR][1000 genomes]
rs9876196	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
2	nsv829773	chr3:161150422-161315189	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv829774	chr3:161229405-161386919	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2422309	chr3:161242389-161425932	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv877711	chr3:161275848-161486665	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 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	chr3:161286800-161294800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr3:161287000-161294600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr3:161289600-161294200	Weak transcription	Fetal Muscle Leg	muscle
4	chr3:161292000-161299600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:161292400-161299200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:161292800-161294000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr3:161293200-161294200	Weak transcription	Colon Smooth Muscle	Colon
8	chr3:161293200-161295000	Enhancers	HUES48 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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