Variant report

Variant	rs313719
Chromosome Location	chr1:86256732-86256733
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12136742	1.00[YRI][hapmap]
rs193398	0.87[CHB][hapmap]
rs1977331	0.87[CHB][hapmap]
rs313699	0.84[AFR][1000 genomes]
rs313710	0.91[CHB][hapmap];0.84[MEX][hapmap];0.80[MKK][hapmap];0.84[AMR][1000 genomes]
rs313713	0.85[AMR][1000 genomes]
rs313732	0.90[CHB][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes]
rs313733	0.87[CHB][hapmap]
rs313734	0.91[CHB][hapmap];0.84[MEX][hapmap]
rs313736	0.83[AMR][1000 genomes]
rs366187	0.91[CHB][hapmap]
rs380654	0.91[CHB][hapmap];0.82[AMR][1000 genomes]
rs412328	0.83[CHB][hapmap]
rs414143	0.82[AMR][1000 genomes]
rs432168	0.83[CHB][hapmap]
rs486417	0.87[CHB][hapmap]
rs4912448	0.95[LWK][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap]
rs4912450	1.00[YRI][hapmap]
rs598104	0.91[CHB][hapmap]
rs673506	0.87[CHB][hapmap]
rs997439	1.00[YRI][hapmap]

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	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv3391173	chr1:86005637-86337469	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv817212	chr1:86127851-86658426	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv546721	chr1:86226352-86392577	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv999743	chr1:86241246-86364846	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs313719	LOC339524	cis	parietal	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86254800-86256800	Weak transcription	Fetal Lung	lung
2	chr1:86255200-86257600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:86256000-86257400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:86256400-86257200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:86256600-86257400	Strong transcription	Primary hematopoietic stem cells	blood

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