Variant report

Variant	rs10519819
Chromosome Location	chr4:147688226-147688227
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10519821	1.00[EUR][1000 genomes]
rs10519826	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10519850	0.97[EUR][1000 genomes]
rs12500369	1.00[EUR][1000 genomes]
rs12501579	1.00[EUR][1000 genomes]
rs12502103	0.97[EUR][1000 genomes]
rs12505022	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12511968	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12512057	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1370303	0.97[EUR][1000 genomes]
rs17021947	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17021951	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17021983	1.00[CEU][hapmap];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17021984	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17022031	1.00[EUR][1000 genomes]
rs17609789	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17609810	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17609942	1.00[EUR][1000 genomes]
rs17609956	1.00[EUR][1000 genomes]
rs17656106	1.00[EUR][1000 genomes]
rs35085760	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs41280531	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4835054	1.00[EUR][1000 genomes]
rs4835344	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4835345	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4835347	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4835350	1.00[EUR][1000 genomes]
rs4835351	1.00[EUR][1000 genomes]
rs4835353	1.00[EUR][1000 genomes]
rs57054230	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57587608	0.97[EUR][1000 genomes]
rs6814899	1.00[EUR][1000 genomes]
rs6819665	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6830880	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6832643	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6836696	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6846438	1.00[EUR][1000 genomes]
rs6857108	1.00[EUR][1000 genomes];0.82[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	nsv461675	chr4:147116864-147768206	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv595651	chr4:147116864-147768206	Weak transcription Enhancers Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv880239	chr4:147666797-147779999	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
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