Variant report

Variant	rs73098385
Chromosome Location	chr4:18616136-18616137
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs59154793	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73098376	1.00[AMR][1000 genomes]
rs73098378	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73098388	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73098389	1.00[AMR][1000 genomes]
rs73098400	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73098402	0.93[AFR][1000 genomes]
rs73100313	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73100316	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73100322	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73100328	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73100391	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73100392	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73100398	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73102316	0.82[AFR][1000 genomes]
rs73102348	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003931	chr4:18241575-18849898	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv533087	chr4:18362040-19176896	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv532708	chr4:18596861-19176896	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:18611000-18619000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:18615400-18616200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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