Variant report

Variant	rs17059276
Chromosome Location	chr13:61617057-61617058
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10507661	1.00[AFR][1000 genomes]
rs10507662	1.00[AFR][1000 genomes]
rs17059292	1.00[AFR][1000 genomes]
rs17059306	1.00[AFR][1000 genomes]
rs17059308	1.00[AFR][1000 genomes]
rs4476064	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73205840	1.00[AFR][1000 genomes]
rs73205850	1.00[AFR][1000 genomes]
rs73205852	1.00[AFR][1000 genomes]
rs73205855	1.00[AFR][1000 genomes]
rs73205856	1.00[AFR][1000 genomes]
rs73205861	1.00[AFR][1000 genomes]
rs73205865	1.00[AFR][1000 genomes]
rs73205866	1.00[AFR][1000 genomes]
rs73205873	1.00[AFR][1000 genomes]
rs73205880	1.00[AFR][1000 genomes]
rs9317156	1.00[AFR][1000 genomes]
rs9563860	1.00[AFR][1000 genomes]
rs9563861	1.00[AFR][1000 genomes]
rs9563863	1.00[AFR][1000 genomes]
rs9563864	1.00[AFR][1000 genomes]
rs9563865	1.00[AFR][1000 genomes]
rs9563866	1.00[AFR][1000 genomes]
rs9563867	1.00[AFR][1000 genomes]
rs9570425	1.00[AFR][1000 genomes]
rs9570426	1.00[AFR][1000 genomes]
rs9570427	1.00[AFR][1000 genomes]
rs9570429	1.00[AFR][1000 genomes]
rs9570431	1.00[AFR][1000 genomes]
rs9570432	1.00[AFR][1000 genomes]
rs9570434	1.00[AFR][1000 genomes]
rs9570438	1.00[AFR][1000 genomes]
rs9570440	1.00[AFR][1000 genomes]
rs9570444	1.00[AFR][1000 genomes]
rs9570446	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	nsv832626	chr13:61545191-61698233	Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61603600-61620400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:61614800-61619400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr13:61616800-61617800	Enhancers	Fetal Heart	heart
4	chr13:61617000-61617400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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