Variant report

Variant	rs37875
Chromosome Location	chr7:78429428-78429429
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1012955	0.87[CEU][hapmap]
rs10244070	0.87[CEU][hapmap]
rs10953690	0.87[CEU][hapmap]
rs1207863	0.87[CEU][hapmap]
rs1207864	0.87[CEU][hapmap]
rs1207865	0.87[CEU][hapmap]
rs1207866	0.87[CEU][hapmap]
rs1207867	0.87[CEU][hapmap]
rs1207894	0.87[CEU][hapmap]
rs12705771	0.87[CEU][hapmap]
rs17151530	1.00[CEU][hapmap]
rs1989977	0.87[CEU][hapmap]
rs1989978	0.87[CEU][hapmap]
rs246463	1.00[CEU][hapmap]
rs246464	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs2525808	0.87[CEU][hapmap]
rs2774059	0.87[CEU][hapmap]
rs37847	0.87[CEU][hapmap]
rs37848	0.87[CEU][hapmap]
rs37850	0.87[CEU][hapmap]
rs37860	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs37862	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs37863	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs37865	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs37868	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs37871	1.00[CEU][hapmap]
rs37872	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs37873	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs37877	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs37881	0.91[EUR][1000 genomes]
rs37882	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37884	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs37887	0.87[CEU][hapmap]
rs39731	1.00[CEU][hapmap]
rs57179939	0.92[ASN][1000 genomes]
rs7780363	0.87[CEU][hapmap]
rs886472	0.87[CEU][hapmap]
rs886473	0.87[CEU][hapmap]
rs886474	0.87[CEU][hapmap]
rs970757	0.87[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv607657	chr7:78329795-78483211	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv949647	chr7:78406281-78495913	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	chr7:78428600-78429600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:78428800-78429600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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