Variant report

Variant	rs587260
Chromosome Location	chr6:54214960-54214961
allele	C/T
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:53)

rs_ID	r²[population]
rs1150876	1.00[EUR][1000 genomes]
rs1150879	1.00[EUR][1000 genomes]
rs1150881	1.00[EUR][1000 genomes]
rs1150882	1.00[EUR][1000 genomes]
rs1150883	1.00[EUR][1000 genomes]
rs1150885	1.00[EUR][1000 genomes]
rs11966518	1.00[EUR][1000 genomes]
rs12664738	1.00[EUR][1000 genomes]
rs1280853	1.00[EUR][1000 genomes]
rs1280855	1.00[EUR][1000 genomes]
rs1280856	1.00[EUR][1000 genomes]
rs1290258	1.00[EUR][1000 genomes]
rs1298874	1.00[EUR][1000 genomes]
rs1340669	1.00[EUR][1000 genomes]
rs1508639	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1614889	1.00[EUR][1000 genomes]
rs1775795	1.00[EUR][1000 genomes]
rs2754784	1.00[EUR][1000 genomes]
rs2754789	1.00[EUR][1000 genomes]
rs2754799	1.00[EUR][1000 genomes]
rs2754800	1.00[EUR][1000 genomes]
rs2754803	1.00[EUR][1000 genomes]
rs2754805	1.00[EUR][1000 genomes]
rs2754806	1.00[EUR][1000 genomes]
rs2754807	1.00[EUR][1000 genomes]
rs2754810	1.00[EUR][1000 genomes]
rs2754811	1.00[EUR][1000 genomes]
rs2792626	1.00[EUR][1000 genomes]
rs2792628	1.00[EUR][1000 genomes]
rs2792632	1.00[EUR][1000 genomes]
rs2792637	1.00[EUR][1000 genomes]
rs2792639	1.00[EUR][1000 genomes]
rs2792640	1.00[EUR][1000 genomes]
rs2792642	1.00[EUR][1000 genomes]
rs2792643	1.00[EUR][1000 genomes]
rs2792645	1.00[EUR][1000 genomes]
rs2792647	1.00[EUR][1000 genomes]
rs2792648	1.00[EUR][1000 genomes]
rs2792651	1.00[EUR][1000 genomes]
rs2792653	1.00[EUR][1000 genomes]
rs2792654	1.00[EUR][1000 genomes]
rs2792658	1.00[EUR][1000 genomes]
rs28878486	1.00[EUR][1000 genomes]
rs507257	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56843634	1.00[EUR][1000 genomes]
rs58779855	1.00[EUR][1000 genomes]
rs59853271	1.00[EUR][1000 genomes]
rs61111674	1.00[EUR][1000 genomes]
rs6458981	1.00[EUR][1000 genomes]
rs685700	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6910818	1.00[EUR][1000 genomes]
rs693027	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73741495	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067663	chr6:53796341-54449718	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529158	chr6:53796341-54449718	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv885888	chr6:54132353-54266032	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54211800-54256200	Weak transcription	Fetal Intestine Large	intestine
2	chr6:54212000-54257400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr6:54212800-54225000	Weak transcription	Fetal Intestine Small	intestine

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