Variant report

Variant	rs73447256
Chromosome Location	chr13:29769929-29769930
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs17072891	1.00[AMR][1000 genomes]
rs17072909	1.00[AMR][1000 genomes]
rs17073120	1.00[AMR][1000 genomes]
rs2992387	1.00[AMR][1000 genomes]
rs59851018	1.00[AMR][1000 genomes]
rs60075430	1.00[AMR][1000 genomes]
rs60351466	1.00[AMR][1000 genomes]
rs61365746	1.00[AMR][1000 genomes]
rs7139933	1.00[AMR][1000 genomes]
rs7317620	1.00[AMR][1000 genomes]
rs7325573	1.00[AMR][1000 genomes]
rs7328204	1.00[AMR][1000 genomes]
rs7332404	1.00[AMR][1000 genomes]
rs7333330	1.00[AMR][1000 genomes]
rs7334265	1.00[AMR][1000 genomes]
rs7337486	1.00[AMR][1000 genomes]
rs73445195	1.00[AMR][1000 genomes]
rs73445200	1.00[AMR][1000 genomes]
rs73447205	1.00[AMR][1000 genomes]
rs73447209	1.00[AMR][1000 genomes]
rs73447227	1.00[AMR][1000 genomes]
rs73447239	1.00[AMR][1000 genomes]
rs73447246	1.00[AMR][1000 genomes]
rs73447249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73447253	1.00[AMR][1000 genomes]
rs73449314	1.00[AMR][1000 genomes]
rs73449318	1.00[AMR][1000 genomes]
rs73449368	1.00[AMR][1000 genomes]
rs73449378	1.00[AMR][1000 genomes]
rs73449379	1.00[AMR][1000 genomes]
rs7995580	1.00[AMR][1000 genomes]
rs7997357	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv3406145	chr13:29616606-29917459	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv899957	chr13:29720732-29820422	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv427927	chr13:29729315-30062054	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv899958	chr13:29752497-29820422	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv899959	chr13:29752497-29832613	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv976	chr13:29759458-29804146	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29763000-29775600	Weak transcription	Aorta	Aorta
2	chr13:29769600-29771000	Enhancers	GM12878-XiMat	blood
3	chr13:29769800-29770200	Enhancers	Fetal Heart	heart
4	chr13:29769800-29771000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr13:29769800-29771200	Enhancers	Primary B cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links