Variant report

Variant	rs73758573
Chromosome Location	chr6:78000387-78000388
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:38)

rs_ID	r²[population]
rs1557159	0.83[ASN][1000 genomes]
rs16888657	0.86[AMR][1000 genomes]
rs16888750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs16888753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1974363	0.83[ASN][1000 genomes]
rs2153889	0.83[ASN][1000 genomes]
rs3934417	0.83[ASN][1000 genomes]
rs55737033	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55950973	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56045818	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs56293001	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56330160	0.97[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs57360632	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs57622060	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs58203810	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58378053	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58682903	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs59685275	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60619744	0.86[AMR][1000 genomes]
rs6453975	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6453976	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6904677	0.83[ASN][1000 genomes]
rs73758553	0.93[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73758572	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73758577	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73758579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73758581	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73758582	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73758583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73758585	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73758587	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73758590	0.93[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73758595	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs73758596	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs73760607	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9341662	0.83[ASN][1000 genomes]
rs9352475	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs947732	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017082	chr6:77585310-78258237	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv534282	chr6:77764575-78351994	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1034979	chr6:77781244-78426249	Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538324	chr6:77781244-78426249	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2753543	chr6:77791848-78059351	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1015307	chr6:77902559-78352291	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77990800-78000400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:77999000-78005400	Enhancers	HUVEC	blood vessel
3	chr6:77999400-78000400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:77999800-78002000	Enhancers	NHEK	skin
5	chr6:78000000-78001200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:78000000-78002800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:78000000-78003800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:78000200-78000600	Enhancers	NHDF-Ad	bronchial
9	chr6:78000200-78000800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:78000200-78002400	Enhancers	HMEC	breast

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