Variant report

Variant	rs73113837
Chromosome Location	chr4:28272843-28272844
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1391220	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1846118	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2309737	1.00[AMR][1000 genomes]
rs57371365	1.00[EUR][1000 genomes]
rs57581586	1.00[EUR][1000 genomes]
rs58411582	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59589574	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60588324	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6825071	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6848787	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73113835	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73113851	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73113868	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73113871	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73113873	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73115433	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73115434	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73115445	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73115466	1.00[AFR][1000 genomes]
rs73122785	0.85[EUR][1000 genomes]
rs73122788	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73124715	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9685431	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005382	chr4:28157180-28403800	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv878775	chr4:28163856-28473048	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1000514	chr4:28192982-28445194	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv878777	chr4:28208093-28343903	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv878778	chr4:28237783-28343903	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1012210	chr4:28246489-28419673	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv878779	chr4:28264394-28343903	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv967981	chr4:28272442-28281577	Enhancers Weak transcription Flanking Active TSS Active TSS	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	chr4:28235000-28279200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:28272600-28279000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links