Variant report

Variant	rs61355480
Chromosome Location	chr4:148625595-148625596
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:148604171..148605724-chr4:148624348..148626339,2	K562	blood:

Variant related genes	Relation type
ENSG00000164169	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10011891	0.83[AMR][1000 genomes]
rs10023419	0.83[AMR][1000 genomes]
rs10029636	0.83[AMR][1000 genomes]
rs10034181	0.83[AMR][1000 genomes]
rs11931510	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11932755	1.00[AMR][1000 genomes]
rs11932883	1.00[AMR][1000 genomes]
rs17023581	0.85[AMR][1000 genomes]
rs28416885	0.83[AMR][1000 genomes]
rs28579791	0.83[AMR][1000 genomes]
rs28676674	0.85[AMR][1000 genomes]
rs34001293	1.00[AMR][1000 genomes]
rs57632432	1.00[AMR][1000 genomes]
rs58012022	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58285779	1.00[AMR][1000 genomes]
rs58965352	0.83[AMR][1000 genomes]
rs59938265	1.00[AMR][1000 genomes]
rs61312957	1.00[AMR][1000 genomes]
rs61363583	1.00[AMR][1000 genomes]
rs72945871	1.00[AMR][1000 genomes]
rs72945873	1.00[AMR][1000 genomes]
rs72945877	1.00[AMR][1000 genomes]
rs72945879	1.00[AMR][1000 genomes]
rs72945896	1.00[AMR][1000 genomes]
rs72947812	1.00[AMR][1000 genomes]
rs72947824	1.00[AMR][1000 genomes]
rs72947833	1.00[AMR][1000 genomes]
rs72947849	1.00[AMR][1000 genomes]
rs72947870	1.00[AMR][1000 genomes]
rs72947876	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72947892	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949789	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949795	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949796	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949798	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs72951406	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs72951412	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs72951422	0.83[AMR][1000 genomes]
rs72951423	0.83[AMR][1000 genomes]
rs72953473	0.83[AMR][1000 genomes]
rs72953477	0.83[AMR][1000 genomes]
rs72953481	0.83[AMR][1000 genomes]
rs72953502	0.83[AMR][1000 genomes]
rs72955506	0.83[AMR][1000 genomes]
rs9993312	0.85[AMR][1000 genomes]
rs9996365	0.83[AMR][1000 genomes]
rs9997304	0.83[AMR][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	nsv1028958	chr4:148377752-148793485	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv498083	chr4:148519825-148917583	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148622800-148626400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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