Variant report

Variant	rs9527126
Chromosome Location	chr13:54267318-54267319
allele	A/G
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:12)

rs_ID	r²[population]
rs11620301	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1336931	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1415162	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34201909	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9316643	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9316644	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9316645	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9316646	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9536495	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9536496	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9536497	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9536510	0.90[EUR][1000 genomes];0.95[ASN][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	nsv1044137	chr13:54124103-54521120	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv541777	chr13:54124103-54521120	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv900091	chr13:54182173-54272104	Enhancers Weak transcription Active TSS ZNF genes & repeats	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	chr13:54265800-54269200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr13:54266000-54268800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr13:54266000-54269000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr13:54266000-54269000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr13:54266000-54269200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr13:54266000-54269200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr13:54266000-54287200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr13:54266200-54268800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr13:54266200-54268800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr13:54266200-54268800	Weak transcription	iPS-20b 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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