Variant report

Variant	rs13438320
Chromosome Location	chr7:21087908-21087909
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10230337	0.89[EUR][1000 genomes]
rs10241014	0.94[EUR][1000 genomes]
rs1024727	0.94[EUR][1000 genomes]
rs10248415	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs10262607	0.94[EUR][1000 genomes]
rs11761249	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12532874	0.94[EUR][1000 genomes]
rs12537929	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12539026	0.94[EUR][1000 genomes]
rs13222046	0.92[EUR][1000 genomes]
rs17143831	0.94[EUR][1000 genomes]
rs17678624	0.94[EUR][1000 genomes]
rs1990465	0.94[EUR][1000 genomes]
rs1990466	0.92[EUR][1000 genomes]
rs56111049	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6955142	0.92[EUR][1000 genomes]
rs7789102	0.91[EUR][1000 genomes]
rs9886061	0.90[EUR][1000 genomes]
rs9886119	0.94[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	nsv830920	chr7:21014535-21201580	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	esv3478244	chr7:21044211-21417347	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3478245	chr7:21044211-21417347	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1020852	chr7:21060791-21375050	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv538799	chr7:21060791-21375050	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:21081800-21094200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:21083200-21098000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:21087800-21089000	Weak transcription	iPS DF 6.9 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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