Variant report

Variant	rs765075
Chromosome Location	chr5:106625115-106625116
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10058308	1.00[EUR][1000 genomes]
rs10062445	1.00[EUR][1000 genomes]
rs10077806	1.00[EUR][1000 genomes]
rs10515370	1.00[ASN][1000 genomes]
rs10515372	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11948860	1.00[ASN][1000 genomes]
rs13163748	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13165897	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13167605	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13169680	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13179809	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13179824	1.00[EUR][1000 genomes]
rs13184636	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13184643	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13184806	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13186418	1.00[ASN][1000 genomes]
rs17159641	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159693	0.99[EUR][1000 genomes]
rs17159727	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159745	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159751	1.00[ASN][1000 genomes]
rs17343335	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17343762	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17400404	1.00[ASN][1000 genomes]
rs17401032	0.91[EUR][1000 genomes]
rs17402238	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17403350	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1895462	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34319558	0.83[EUR][1000 genomes]
rs35307227	1.00[EUR][1000 genomes]
rs35709847	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35740714	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35748495	1.00[ASN][1000 genomes]
rs35775035	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55849939	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56283997	1.00[ASN][1000 genomes]
rs56852743	1.00[EUR][1000 genomes]
rs60635486	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6596736	1.00[EUR][1000 genomes]
rs66460437	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67504033	1.00[ASN][1000 genomes]
rs67878207	0.83[EUR][1000 genomes]
rs6897756	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72784111	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72784113	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7701101	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7711216	1.00[ASN][1000 genomes]
rs7711298	0.83[EUR][1000 genomes]
rs7730647	0.80[EUR][1000 genomes]
rs7735115	0.99[EUR][1000 genomes]
rs9327996	1.00[EUR][1000 genomes]
rs9327997	1.00[EUR][1000 genomes]

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	nsv1030118	chr5:106006097-106847949	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv823170	chr5:106326293-106673695	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1034276	chr5:106461538-106944163	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv537851	chr5:106461538-106944163	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106621600-106625600	Weak transcription	Pancreas	Pancrea
2	chr5:106621600-106626600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:106621800-106636600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:106623400-106626200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr5:106623800-106625400	Enhancers	Fetal Heart	heart
6	chr5:106624400-106625400	Enhancers	Brain Substantia Nigra	brain
7	chr5:106624400-106625800	Enhancers	Primary B cells from peripheral blood	blood
8	chr5:106624600-106625400	Flanking Active TSS	GM12878-XiMat	blood
9	chr5:106624600-106625600	Enhancers	Primary B cells from cord blood	blood
10	chr5:106624600-106625800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr5:106624800-106625400	Enhancers	Brain Hippocampus Middle	brain
12	chr5:106624800-106625400	Enhancers	HMEC	breast
13	chr5:106625000-106627200	Enhancers	Stomach Mucosa	stomach

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