Variant report

Variant	rs9571691
Chromosome Location	chr13:67490376-67490377
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:67483833..67485636-chr13:67488451..67490558,2	MCF-7	breast:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11618220	0.98[ASN][1000 genomes]
rs11841902	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12427700	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12429002	0.87[EUR][1000 genomes]
rs12430583	0.94[EUR][1000 genomes]
rs12875741	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28459050	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34304003	0.87[EUR][1000 genomes]
rs34948729	0.94[ASN][1000 genomes]
rs4884707	0.93[EUR][1000 genomes]
rs7324151	0.94[EUR][1000 genomes]
rs9564358	0.94[EUR][1000 genomes]
rs9564359	0.97[ASN][1000 genomes]
rs9564360	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9564361	0.94[ASN][1000 genomes]
rs9564362	0.94[ASN][1000 genomes]
rs9564363	0.92[ASN][1000 genomes]
rs9571685	0.87[EUR][1000 genomes]
rs9571686	0.91[EUR][1000 genomes]
rs9571687	0.94[EUR][1000 genomes]
rs9571688	0.93[EUR][1000 genomes]
rs9571692	0.94[ASN][1000 genomes]
rs9571693	0.94[ASN][1000 genomes]
rs9571694	0.94[ASN][1000 genomes]
rs9571695	0.94[ASN][1000 genomes]
rs9571696	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041133	chr13:66723731-67530595	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv530605	chr13:67126136-67697306	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1035741	chr13:67212973-68077950	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv541817	chr13:67212973-68077950	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv523360	chr13:67322714-67520344	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1051576	chr13:67322747-67520255	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv900406	chr13:67434161-67532205	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv900407	chr13:67434161-67603745	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv562138	chr13:67455787-67511430	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv832640	chr13:67460304-67635966	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv428604	chr13:67480426-67645030	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67487600-67490800	Weak transcription	Brain Angular Gyrus	brain
2	chr13:67489000-67490400	Enhancers	HUVEC	blood vessel
3	chr13:67489400-67491600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr13:67489600-67490400	Flanking Active TSS	Dnd41	blood
5	chr13:67489600-67490600	Enhancers	Brain Anterior Caudate	brain
6	chr13:67489600-67491400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr13:67489800-67490400	Weak transcription	Brain Substantia Nigra	brain
8	chr13:67490000-67490600	Enhancers	Brain Hippocampus Middle	brain
9	chr13:67490000-67500200	Weak transcription	Primary B cells from cord blood	blood
10	chr13:67490000-67500400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr13:67490200-67491200	Enhancers	Primary T cells from cord blood	blood
12	chr13:67490200-67491200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr13:67490200-67492200	Enhancers	A549	lung
14	chr13:67490200-67500200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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