Variant report

Variant	rs73129305
Chromosome Location	chr5:92501084-92501085
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs58235673	0.95[AFR][1000 genomes]
rs60715197	0.95[AFR][1000 genomes]
rs73129314	0.95[AFR][1000 genomes]
rs73129321	0.95[AFR][1000 genomes]
rs73146877	1.00[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029175	chr5:92436038-92548473	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92498600-92501400	Enhancers	Muscle Satellite Cultured Cells	--
2	chr5:92499000-92501600	Enhancers	NHEK	skin
3	chr5:92499400-92501400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:92499400-92501400	Enhancers	HUVEC	blood vessel
5	chr5:92499400-92501800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr5:92500800-92521600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:92501000-92501600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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