Variant report

Variant	rs73109081
Chromosome Location	chr4:19695051-19695052
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16868689	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56672156	1.00[AMR][1000 genomes]
rs57626495	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57879648	1.00[AMR][1000 genomes]
rs58108305	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59483698	1.00[AMR][1000 genomes]
rs73092817	1.00[AMR][1000 genomes]
rs73097638	1.00[AMR][1000 genomes]
rs73097664	1.00[AMR][1000 genomes]
rs73101137	1.00[AMR][1000 genomes]
rs73101146	1.00[AMR][1000 genomes]
rs73101175	1.00[AMR][1000 genomes]
rs73101201	1.00[AMR][1000 genomes]
rs73103103	1.00[AMR][1000 genomes]
rs73103109	1.00[AMR][1000 genomes]
rs73103120	1.00[AMR][1000 genomes]
rs73103123	1.00[AMR][1000 genomes]
rs73111003	1.00[AMR][1000 genomes]
rs73111007	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878733	chr4:19335464-19928602	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv461286	chr4:19488871-19709795	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv593786	chr4:19488871-19709795	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv829873	chr4:19582263-19742515	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv829874	chr4:19635213-19781102	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv529290	chr4:19658583-20173839	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19686200-19695800	Weak transcription	Fetal Lung	lung
2	chr4:19686600-19695800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr4:19692000-19695800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:19692000-19696000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:19692200-19695800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:19694400-19695200	Weak transcription	Dnd41	blood
7	chr4:19694400-19695800	Weak transcription	Fetal Kidney	kidney
8	chr4:19694400-19695800	Weak transcription	NHDF-Ad	bronchial
9	chr4:19694600-19696000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:19694800-19696200	Enhancers	Colon Smooth Muscle	Colon
11	chr4:19695000-19697000	Enhancers	Fetal Stomach	stomach

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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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