Variant report

Variant	rs10147344
Chromosome Location	chr14:37513907-37513908
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10132291	0.93[AFR][1000 genomes]
rs10136142	1.00[AMR][1000 genomes]
rs10139375	1.00[AMR][1000 genomes]
rs10139658	1.00[AMR][1000 genomes]
rs10143006	1.00[AMR][1000 genomes]
rs10145879	1.00[AMR][1000 genomes]
rs10147578	1.00[AMR][1000 genomes]
rs10150081	1.00[AMR][1000 genomes]
rs10152058	1.00[AMR][1000 genomes]
rs28576870	1.00[AMR][1000 genomes]
rs28659794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60763979	1.00[AMR][1000 genomes]
rs7155771	1.00[AMR][1000 genomes]
rs74045204	1.00[AMR][1000 genomes]
rs74045464	1.00[AMR][1000 genomes]
rs74047035	1.00[AMR][1000 genomes]
rs8018385	1.00[AMR][1000 genomes]
rs9322972	1.00[AMR][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	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1036201	chr14:37498841-37542041	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1037719	chr14:37498841-37546359	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv526786	chr14:37499904-37537352	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1048854	chr14:37505438-37546359	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37510600-37514000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:37512800-37516400	Weak transcription	Aorta	Aorta

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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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