Variant report

Variant	rs917032
Chromosome Location	chr11:17790227-17790228
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:17789104..17793559-chr11:17796092..17800270,5	MCF-7	breast:
2	chr11:17783850..17786298-chr11:17789626..17792965,4	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1003921	0.87[CEU][hapmap]
rs10444223	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10444224	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10766435	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11024393	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs16934680	0.89[ASN][1000 genomes]
rs3893215	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs56037689	0.89[ASN][1000 genomes]
rs56205256	0.89[ASN][1000 genomes]
rs59267268	0.89[ASN][1000 genomes]
rs6486396	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7110441	0.89[ASN][1000 genomes]
rs7114718	0.89[ASN][1000 genomes]
rs7124411	0.89[ASN][1000 genomes]
rs7124999	0.89[ASN][1000 genomes]
rs71457882	1.00[ASN][1000 genomes]
rs73424016	0.89[ASN][1000 genomes]
rs7924746	0.89[ASN][1000 genomes]
rs7926535	0.89[ASN][1000 genomes]
rs7942518	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv467717	chr11:17713507-17791822	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv553588	chr11:17713507-17791822	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1038119	chr11:17744915-17794577	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv467718	chr11:17744992-17809724	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
5	nsv553589	chr11:17744992-17809724	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
6	nsv516767	chr11:17758587-17809724	Bivalent Enhancer Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
7	nsv832078	chr11:17780503-17953521	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
8	nsv1043973	chr11:17781560-17869896	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17772400-17790600	Weak transcription	Right Atrium	heart
2	chr11:17773400-17795600	Weak transcription	Brain Hippocampus Middle	brain
3	chr11:17774000-17791600	Weak transcription	Pancreas	Pancrea
4	chr11:17783400-17791600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr11:17787800-17796000	Weak transcription	Brain Cingulate Gyrus	brain
6	chr11:17787800-17801400	Weak transcription	Brain Angular Gyrus	brain
7	chr11:17788000-17791400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:17788000-17791600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr11:17788000-17791600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:17788000-17795800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr11:17788000-17811400	Weak transcription	Brain Anterior Caudate	brain
12	chr11:17788200-17793000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr11:17788200-17793000	Weak transcription	Brain Germinal Matrix	brain
14	chr11:17788200-17793400	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr11:17788400-17791600	Weak transcription	Fetal Intestine Large	intestine
16	chr11:17788400-17791800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:17788400-17802000	Weak transcription	Fetal Brain Male	brain
18	chr11:17790200-17792600	Weak transcription	Fetal Brain Female	brain

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