Variant report

Variant	rs13426558
Chromosome Location	chr2:64275819-64275820
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:64275419..64277085-chr2:64280616..64282779,2	K562	blood:
2	chr2:64275467..64277323-chr2:64280220..64283208,2	MCF-7	breast:
3	chr2:64267308..64269461-chr2:64274492..64276041,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10170601	1.00[AMR][1000 genomes]
rs10175439	1.00[AMR][1000 genomes]
rs10178275	1.00[AMR][1000 genomes]
rs10179276	1.00[AMR][1000 genomes]
rs10181595	1.00[AMR][1000 genomes]
rs10194235	1.00[AMR][1000 genomes]
rs10197962	1.00[AMR][1000 genomes]
rs13384491	1.00[AMR][1000 genomes]
rs13386653	1.00[AMR][1000 genomes]
rs13387854	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13391343	1.00[AMR][1000 genomes]
rs13394672	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13396651	1.00[AMR][1000 genomes]
rs13402981	1.00[AMR][1000 genomes]
rs13403474	1.00[AMR][1000 genomes]
rs13405024	1.00[AMR][1000 genomes]
rs13411468	1.00[AMR][1000 genomes]
rs13415878	1.00[AMR][1000 genomes]
rs13416589	1.00[AMR][1000 genomes]
rs13418689	1.00[AMR][1000 genomes]
rs13422518	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13423144	1.00[AMR][1000 genomes]
rs13425328	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13425693	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13426789	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13427671	1.00[AMR][1000 genomes]
rs13427994	1.00[AMR][1000 genomes]
rs13428769	1.00[AMR][1000 genomes]
rs13429652	1.00[AMR][1000 genomes]
rs13431823	1.00[AMR][1000 genomes]
rs6742704	1.00[AMR][1000 genomes]
rs7579814	1.00[AMR][1000 genomes]
rs7587919	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531376	chr2:64094322-64521876	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	esv2763643	chr2:64219887-64281337	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1013132	chr2:64235175-64631084	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats 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	40 gene(s)	inside rSNPs	diseases
4	esv2757803	chr2:64253005-64539556	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	esv2759055	chr2:64253005-64539556	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv428396	chr2:64253005-64539556	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 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	chr2:64268000-64276800	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr2:64268200-64276600	Weak transcription	Fetal Thymus	thymus
3	chr2:64273600-64276800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:64275200-64276600	Weak transcription	Primary T cells from cord blood	blood
5	chr2:64275600-64278800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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