Variant report

Variant	rs57787929
Chromosome Location	chr14:65594194-65594195
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11844303	1.00[EUR][1000 genomes]
rs11849905	1.00[EUR][1000 genomes]
rs1256502	1.00[EUR][1000 genomes]
rs17102412	1.00[EUR][1000 genomes]
rs57140560	1.00[EUR][1000 genomes]
rs7149107	1.00[EUR][1000 genomes]
rs7160535	1.00[EUR][1000 genomes]
rs73270897	1.00[EUR][1000 genomes]
rs73272693	1.00[EUR][1000 genomes]
rs74056658	1.00[EUR][1000 genomes]
rs74056660	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv832816	chr14:65473244-65644645	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 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	chr14:65593400-65594200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:65593400-65594200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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