Variant report

Variant	rs37887
Chromosome Location	chr7:78438407-78438408
allele	C/T
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:39)

rs_ID	r²[population]
rs1012955	1.00[ASN][1000 genomes]
rs10244070	1.00[ASN][1000 genomes]
rs1029495	1.00[ASN][1000 genomes]
rs10953690	1.00[ASN][1000 genomes]
rs1207863	1.00[ASN][1000 genomes]
rs1207864	1.00[ASN][1000 genomes]
rs1207865	1.00[ASN][1000 genomes]
rs1207866	1.00[ASN][1000 genomes]
rs1207867	1.00[ASN][1000 genomes]
rs1207894	1.00[ASN][1000 genomes]
rs1211415	1.00[ASN][1000 genomes]
rs12705771	1.00[ASN][1000 genomes]
rs17151530	0.87[CEU][hapmap]
rs1989977	1.00[ASN][1000 genomes]
rs1989978	1.00[ASN][1000 genomes]
rs246463	0.87[CEU][hapmap]
rs246464	0.87[CEU][hapmap]
rs2774059	1.00[ASN][1000 genomes]
rs37847	1.00[ASN][1000 genomes]
rs37848	1.00[ASN][1000 genomes]
rs37860	0.87[CEU][hapmap]
rs37862	0.87[CEU][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37863	0.87[CEU][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37865	0.87[CEU][hapmap]
rs37868	0.87[CEU][hapmap]
rs37871	0.87[CEU][hapmap]
rs37872	0.87[CEU][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37873	0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37875	0.87[CEU][hapmap]
rs37877	0.87[CEU][hapmap]
rs37881	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37882	0.80[EUR][1000 genomes]
rs37884	0.87[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs39731	0.87[CEU][hapmap]
rs55917954	1.00[ASN][1000 genomes]
rs7780363	1.00[ASN][1000 genomes]
rs886472	1.00[ASN][1000 genomes]
rs886473	1.00[ASN][1000 genomes]
rs886474	1.00[ASN][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	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
5	nsv1024961	chr7:78432257-78483201	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78434200-78438600	Weak transcription	Ovary	ovary

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