Variant report

Variant	rs861928
Chromosome Location	chr14:37391570-37391571
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12431972	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs12587486	1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1367033	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs1367034	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs1429840	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];0.81[TSI][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17105665	1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17105692	1.00[CEU][hapmap];0.81[JPT][hapmap];0.82[MKK][hapmap];0.88[TSI][hapmap]
rs17105696	1.00[CEU][hapmap];1.00[GIH][hapmap];0.86[MKK][hapmap];0.88[TSI][hapmap]
rs17105720	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17105756	1.00[CEU][hapmap];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17177892	0.91[EUR][1000 genomes]
rs2021932	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2022717	0.82[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs712404	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7145237	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7147105	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs7150167	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs8014926	0.82[CHB][hapmap];0.81[JPT][hapmap];0.91[ASN][1000 genomes]
rs8015456	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs848702	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs861924	1.00[CEU][hapmap];0.90[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap]
rs861925	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.92[YRI][hapmap]
rs9635194	1.00[CEU][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047290	chr14:36564568-37445157	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
2	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

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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