Variant report

Variant	rs3758737
Chromosome Location	chr11:34523968-34523969
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	chr11:34516973..34519937-chr11:34521285..34524160,2	MCF-7	breast:

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10488737	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12418222	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12421999	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16925614	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16925662	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16925668	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16925673	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16925678	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2076556	0.80[EUR][1000 genomes]
rs2231819	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2300182	0.80[EUR][1000 genomes]
rs3758735	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3758736	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3758738	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4755374	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4756146	0.80[EUR][1000 genomes]
rs4756151	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4756155	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4756156	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55633825	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55665450	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55941777	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56291727	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7102889	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7104121	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7104394	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7106485	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7109462	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7109778	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7115064	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7126085	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7126243	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7130331	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7130345	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72923163	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72924903	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72924928	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72927347	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72927368	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72927369	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72927372	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7395059	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7928866	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7935626	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7938373	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][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	nsv897207	chr11:34253683-34621004	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv897208	chr11:34257064-34562247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv897209	chr11:34309519-34548906	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv832114	chr11:34424428-34607851	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv897211	chr11:34514941-34609541	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv897212	chr11:34523173-34621004	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3758737	CAT	cis	Whole Blood	GTEx

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34518400-34534800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:34521200-34524000	Enhancers	Adipose Nuclei	Adipose
3	chr11:34521600-34524400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr11:34521800-34524200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:34522000-34524200	Enhancers	Gastric	stomach
6	chr11:34522400-34524400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr11:34522400-34524600	Enhancers	NH-A	brain
8	chr11:34522600-34524200	Enhancers	NHDF-Ad	bronchial
9	chr11:34522600-34524400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:34522600-34524400	Enhancers	HSMMtube	muscle
11	chr11:34522600-34524600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:34522600-34524600	Enhancers	Liver	Liver
13	chr11:34522600-34524600	Enhancers	Fetal Lung	lung
14	chr11:34522800-34524000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:34522800-34524000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:34522800-34524200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr11:34522800-34524200	Enhancers	Placenta	Placenta
18	chr11:34522800-34524400	Flanking Active TSS	Hela-S3	cervix
19	chr11:34522800-34524400	Enhancers	NHLF	lung
20	chr11:34522800-34524600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr11:34522800-34524600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr11:34523000-34524000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:34523000-34524000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr11:34523000-34524200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr11:34523000-34524200	Enhancers	Brain Anterior Caudate	brain
26	chr11:34523000-34524200	Enhancers	Spleen	Spleen
27	chr11:34523200-34524000	Enhancers	A549	lung
28	chr11:34523200-34524200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:34523200-34524200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:34523200-34524200	Enhancers	Pancreas	Pancrea
31	chr11:34523200-34524200	Enhancers	Stomach Mucosa	stomach
32	chr11:34523200-34524400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr11:34523400-34524000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr11:34523400-34524200	Flanking Active TSS	HepG2	liver
35	chr11:34523600-34524000	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr11:34523600-34524000	Enhancers	Esophagus	oesophagus
37	chr11:34523600-34524000	Flanking Active TSS	HSMM	muscle
38	chr11:34523600-34524200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr11:34523600-34524200	Flanking Active TSS	Osteobl	bone
40	chr11:34523600-34524400	Enhancers	Lung	lung
41	chr11:34523800-34524000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr11:34523800-34524000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr11:34523800-34536800	Weak transcription	Right Atrium	heart

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