Variant report

Variant	rs772
Chromosome Location	chr9:71313549-71313550
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:71312864..71316000-chr9:71317726..71321566,4	MCF-7	breast:
2	chr9:71313421..71317704-chr9:71318350..71323636,8	K562	blood:
3	chr9:71310655..71314334-chr9:71315836..71317946,3	K562	blood:

Variant related genes	Relation type
ENSG00000107242	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10511959	1.00[ASN][1000 genomes]
rs13284137	1.00[ASN][1000 genomes]
rs13288798	1.00[ASN][1000 genomes]
rs13288885	1.00[ASN][1000 genomes]
rs13290124	1.00[ASN][1000 genomes]
rs13297946	1.00[ASN][1000 genomes]
rs17479202	1.00[ASN][1000 genomes]
rs34054758	1.00[ASN][1000 genomes]
rs34206324	1.00[ASN][1000 genomes]
rs34267520	1.00[ASN][1000 genomes]
rs34344868	1.00[ASN][1000 genomes]
rs34412731	1.00[ASN][1000 genomes]
rs34436601	1.00[ASN][1000 genomes]
rs34532945	1.00[ASN][1000 genomes]
rs34763246	1.00[ASN][1000 genomes]
rs35029924	1.00[ASN][1000 genomes]
rs35551873	1.00[ASN][1000 genomes]
rs35596772	1.00[ASN][1000 genomes]
rs35666199	1.00[ASN][1000 genomes]
rs6560237	1.00[ASN][1000 genomes]
rs7045561	1.00[ASN][1000 genomes]
rs7048633	1.00[ASN][1000 genomes]
rs71501771	1.00[ASN][1000 genomes]
rs71503634	1.00[ASN][1000 genomes]
rs7858883	1.00[ASN][1000 genomes]
rs7859065	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	esv2422258	chr9:71234845-71663340	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS 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
7	nsv1017903	chr9:71276951-71690579	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	esv2757339	chr9:71291107-71353743	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv2759693	chr9:71291107-71353743	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	esv2752385	chr9:71304465-71332240	Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71305400-71319400	Weak transcription	Left Ventricle	heart
2	chr9:71305800-71318600	Weak transcription	Fetal Intestine Small	intestine
3	chr9:71312600-71313600	Enhancers	K562	blood
4	chr9:71312600-71313800	Enhancers	Fetal Heart	heart
5	chr9:71313000-71314600	Enhancers	Primary hematopoietic stem cells	blood
6	chr9:71313200-71314000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr9:71313200-71314400	Enhancers	Primary B cells from peripheral blood	blood
8	chr9:71313200-71318600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:71313400-71314400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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