Variant report

Variant	rs11234441
Chromosome Location	chr11:85563065-85563066
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:85561536..85564394-chr11:85565907..85568205,2	K562	blood:
2	chr11:85559798..85561518-chr11:85561594..85563277,2	MCF-7	breast:
3	chr11:85554468..85557167-chr11:85560907..85564178,3	MCF-7	breast:
4	chr11:85562667..85564286-chr11:85564557..85566110,2	MCF-7	breast:
5	chr11:85562706..85564539-chr11:85564547..85566114,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000150676	Chromatin interaction
ENSG00000215504	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10501603	1.00[ASN][1000 genomes]
rs10898431	1.00[ASN][1000 genomes]
rs11234489	1.00[ASN][1000 genomes]
rs11234492	1.00[ASN][1000 genomes]
rs11234496	1.00[ASN][1000 genomes]
rs11234502	1.00[ASN][1000 genomes]
rs11234512	1.00[ASN][1000 genomes]
rs11234513	1.00[ASN][1000 genomes]
rs11234517	1.00[ASN][1000 genomes]
rs11234522	1.00[ASN][1000 genomes]
rs11825378	1.00[ASN][1000 genomes]
rs11825912	1.00[ASN][1000 genomes]
rs11828161	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12278260	1.00[ASN][1000 genomes]
rs12279581	1.00[ASN][1000 genomes]
rs12281958	1.00[ASN][1000 genomes]
rs12287170	1.00[ASN][1000 genomes]
rs17148600	1.00[ASN][1000 genomes]
rs17745153	1.00[ASN][1000 genomes]
rs17745236	1.00[ASN][1000 genomes]
rs17817588	1.00[ASN][1000 genomes]
rs41381550	1.00[ASN][1000 genomes]
rs4944552	1.00[ASN][1000 genomes]
rs56944537	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57125313	1.00[ASN][1000 genomes]
rs58515881	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59019168	1.00[ASN][1000 genomes]
rs59104711	1.00[ASN][1000 genomes]
rs60253048	1.00[ASN][1000 genomes]
rs60264644	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60737637	1.00[ASN][1000 genomes]
rs61535933	1.00[ASN][1000 genomes]
rs72951268	1.00[ASN][1000 genomes]
rs72959177	1.00[ASN][1000 genomes]
rs72959197	1.00[ASN][1000 genomes]
rs72963077	1.00[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	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	nsv832222	chr11:85405712-85603981	Enhancers Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1047147	chr11:85459235-85594800	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv541114	chr11:85459235-85594800	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv1035489	chr11:85502953-85778229	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
9	nsv1048818	chr11:85524635-85746473	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
10	nsv541116	chr11:85524635-85746473	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
11	nsv898051	chr11:85554057-85620823	Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85540000-85565000	Weak transcription	Ovary	ovary
2	chr11:85553400-85563400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:85556400-85564800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:85556600-85565400	Weak transcription	Hela-S3	cervix
5	chr11:85558800-85564800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr11:85559800-85565000	Weak transcription	Osteobl	bone
7	chr11:85560200-85563800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:85560800-85563400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:85561400-85565000	Weak transcription	HMEC	breast
10	chr11:85561600-85563400	Weak transcription	Pancreas	Pancrea
11	chr11:85561800-85565400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr11:85562000-85565600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr11:85562600-85565000	Weak transcription	HSMM	muscle
14	chr11:85563000-85563600	Strong transcription	Fetal Lung	lung
15	chr11:85563000-85565200	Weak transcription	A549	lung

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