Variant report

Variant	rs73114922
Chromosome Location	chr4:27792924-27792925
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs16879698	1.00[EUR][1000 genomes]
rs16879706	1.00[EUR][1000 genomes]
rs16879729	1.00[EUR][1000 genomes]
rs2871292	1.00[EUR][1000 genomes]
rs73112905	1.00[EUR][1000 genomes]
rs73112911	1.00[EUR][1000 genomes]
rs73122935	1.00[EUR][1000 genomes]
rs73122975	1.00[EUR][1000 genomes]
rs73124988	1.00[EUR][1000 genomes]
rs73805752	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	nsv1013877	chr4:27539626-28051576	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv878770	chr4:27680483-27844411	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1012113	chr4:27694978-27819838	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
4	nsv537057	chr4:27694978-27819838	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
5	nsv878771	chr4:27760141-27897437	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:27791200-27793000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:27791200-27793200	Enhancers	Muscle Satellite Cultured Cells	--
3	chr4:27791200-27793600	Enhancers	HMEC	breast
4	chr4:27791400-27793000	Enhancers	NH-A	brain
5	chr4:27791400-27793600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:27792200-27793200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:27792200-27793200	Enhancers	NHEK	skin
8	chr4:27792400-27797000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:27792600-27793600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:27792800-27793000	Enhancers	Placenta Amnion	Placenta Amnion

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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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