Variant report

Variant	rs73303729
Chromosome Location	chr5:124436480-124436481
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs13172601	1.00[AMR][1000 genomes]
rs17152294	1.00[AMR][1000 genomes]
rs6890321	1.00[AMR][1000 genomes]
rs73303731	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303733	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303736	1.00[AMR][1000 genomes]
rs73305853	1.00[AMR][1000 genomes]
rs73305854	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305856	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305857	1.00[AMR][1000 genomes]
rs73305859	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305862	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305867	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305869	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305873	1.00[AMR][1000 genomes]
rs73305876	1.00[AMR][1000 genomes]
rs73305884	1.00[AMR][1000 genomes]
rs73307892	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882822	chr5:124250018-124449375	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830475	chr5:124387292-124550256	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124435000-124439200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:124436200-124436600	Enhancers	Lung	lung
3	chr5:124436200-124437000	Enhancers	Adipose Nuclei	Adipose
4	chr5:124436200-124437000	Enhancers	HUVEC	blood vessel
5	chr5:124436400-124436800	Enhancers	H9 Cell Line	embryonic stem cell
6	chr5:124436400-124436800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr5:124436400-124436800	Enhancers	HUES6 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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