Variant report

Variant	rs71501771
Chromosome Location	chr9:71198224-71198225
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:71198223..71198730-chr9:71614318..71615145,2	MCF-7	breast:
2	chr9:71198182..71198791-chr9:71300404..71301342,2	MCF-7	breast:
3	chr9:71197374..71198367-chr9:71614324..71614982,2	MCF-7	breast:
4	chr9:71191723..71194469-chr9:71195541..71198531,3	K562	blood:

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

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10511959	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13284137	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13288798	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13288885	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13290124	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13296119	1.00[ASN][1000 genomes]
rs13297946	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17479202	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34054758	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34206324	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34267520	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34344868	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34377966	1.00[ASN][1000 genomes]
rs34412731	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34436601	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34532945	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34763246	1.00[ASN][1000 genomes]
rs35029924	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35551873	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35596772	1.00[ASN][1000 genomes]
rs35666199	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6560237	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7045561	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7048633	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71503634	1.00[ASN][1000 genomes]
rs772	1.00[ASN][1000 genomes]
rs7858883	1.00[ASN][1000 genomes]
rs7859065	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893411	chr9:71130848-71199545	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv893412	chr9:71130848-71199545	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1024967	chr9:71130848-71210031	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv482506	chr9:71130848-71280888	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers 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	6 gene(s)	inside rSNPs	diseases
5	nsv466392	chr9:71130848-71318817	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv614546	chr9:71130848-71318817	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1026962	chr9:71130848-71357605	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv1032210	chr9:71130848-71511987	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	nsv893414	chr9:71139378-71320732	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr9:71182800-71199000	Weak transcription	Colon Smooth Muscle	Colon
2	chr9:71194800-71199200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr9:71198000-71199200	Enhancers	Fetal Stomach	stomach

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