Variant report

Variant	rs3218711
Chromosome Location	chr11:108236264-108236265
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:108235117..108237355-chr11:108238293..108240320,2	MCF-7	breast:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11212567	1.00[EUR][1000 genomes]
rs11212571	1.00[EUR][1000 genomes]
rs11212574	1.00[EUR][1000 genomes]
rs11212576	1.00[EUR][1000 genomes]
rs11212582	1.00[EUR][1000 genomes]
rs11212590	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212593	1.00[ASN][1000 genomes]
rs11212595	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212596	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212603	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212651	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11212652	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11212668	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11212670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11212675	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11512449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12360724	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2234993	1.00[EUR][1000 genomes]
rs3092838	1.00[AFR][1000 genomes]
rs3092910	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4987947	1.00[EUR][1000 genomes]
rs4988005	1.00[EUR][1000 genomes]
rs4988007	1.00[EUR][1000 genomes]
rs4988033	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4988047	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4988063	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898383	chr11:108068954-108251211	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv898384	chr11:108097333-108251211	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv1052254	chr11:108122683-108845008	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv541164	chr11:108122683-108845008	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv832262	chr11:108123831-108309350	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv832263	chr11:108183372-108384391	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108094800-108244400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:108212000-108236600	Weak transcription	Stomach Mucosa	stomach
3	chr11:108212200-108241400	Weak transcription	Hela-S3	cervix
4	chr11:108212800-108238000	Weak transcription	HMEC	breast
5	chr11:108220200-108237000	Weak transcription	A549	lung
6	chr11:108222800-108242200	Weak transcription	Fetal Intestine Small	intestine
7	chr11:108224200-108239200	Weak transcription	Small Intestine	intestine
8	chr11:108225400-108243200	Weak transcription	Fetal Heart	heart
9	chr11:108226000-108240200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr11:108226400-108241400	Weak transcription	Thymus	Thymus
11	chr11:108226400-108244200	Weak transcription	Psoas Muscle	Psoas
12	chr11:108226400-108244600	Weak transcription	Gastric	stomach
13	chr11:108226600-108242000	Weak transcription	Lung	lung
14	chr11:108226600-108257400	Weak transcription	Right Ventricle	heart
15	chr11:108226800-108236800	Weak transcription	Colonic Mucosa	Colon
16	chr11:108226800-108237200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:108226800-108239000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:108226800-108239000	Weak transcription	Esophagus	oesophagus
19	chr11:108226800-108241400	Weak transcription	Aorta	Aorta
20	chr11:108226800-108241400	Weak transcription	NHEK	skin
21	chr11:108226800-108242800	Weak transcription	Placenta	Placenta
22	chr11:108226800-108243400	Weak transcription	Fetal Brain Male	brain
23	chr11:108227000-108238600	Weak transcription	Brain Substantia Nigra	brain
24	chr11:108227000-108239200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr11:108227000-108239400	Weak transcription	Brain Cingulate Gyrus	brain
26	chr11:108227200-108240800	Weak transcription	Pancreas	Pancrea
27	chr11:108227200-108241400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr11:108227600-108237800	Weak transcription	Colon Smooth Muscle	Colon
29	chr11:108227600-108240400	Weak transcription	GM12878-XiMat	blood
30	chr11:108227600-108243200	Weak transcription	NH-A	brain
31	chr11:108227600-108245600	Weak transcription	Fetal Brain Female	brain
32	chr11:108227800-108237400	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr11:108227800-108237800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:108227800-108239000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr11:108227800-108239000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr11:108227800-108239600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:108227800-108242000	Weak transcription	Brain Germinal Matrix	brain
38	chr11:108227800-108242800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr11:108227800-108243400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr11:108227800-108243400	Weak transcription	Brain Angular Gyrus	brain
41	chr11:108227800-108243800	Weak transcription	Fetal Kidney	kidney
42	chr11:108227800-108244200	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr11:108227800-108245600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr11:108228200-108239400	Weak transcription	Fetal Stomach	stomach
45	chr11:108233600-108238600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr11:108233800-108238600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr11:108233800-108240000	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr11:108233800-108240200	Strong transcription	Primary T cells from cord blood	blood
49	chr11:108233800-108242400	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr11:108234000-108241000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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