Variant report

Variant	rs17281256
Chromosome Location	chr8:60952675-60952676
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10091969	0.82[EUR][1000 genomes]
rs10092264	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10104844	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10105249	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10113409	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10504304	0.91[EUR][1000 genomes]
rs11986881	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11990259	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11997353	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13439744	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16925552	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16925559	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17279957	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17280265	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17280286	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17280386	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17280559	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17280832	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17281312	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17281361	0.91[EUR][1000 genomes]
rs17344931	0.82[EUR][1000 genomes]
rs17346051	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17346175	0.91[EUR][1000 genomes]
rs17346319	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17346443	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17346637	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28429790	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28483493	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28654982	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28663360	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62509861	0.91[EUR][1000 genomes]
rs62509862	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62511150	0.82[EUR][1000 genomes]
rs62512088	0.91[EUR][1000 genomes]
rs62512128	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62512129	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62512130	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62512131	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62512132	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73682244	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831331	chr8:60770382-60959633	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv917756	chr8:60942299-61862796	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60940000-60968400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:60951600-60953200	Enhancers	Colon Smooth Muscle	Colon
3	chr8:60951600-60953400	Enhancers	Fetal Lung	lung
4	chr8:60952000-60953000	Enhancers	HUVEC	blood vessel
5	chr8:60952200-60953000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:60952200-60953000	Enhancers	Rectal Smooth Muscle	rectum
7	chr8:60952200-60954000	Enhancers	HMEC	breast
8	chr8:60952400-60952800	Weak transcription	Fetal Kidney	kidney
9	chr8:60952400-60953400	Weak transcription	GM12878-XiMat	blood
10	chr8:60952400-60953600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:60952400-60955400	Weak transcription	Fetal Stomach	stomach

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