Variant report

Variant	rs3923033
Chromosome Location	chr6:128479460-128479461
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10499138	0.82[ASN][1000 genomes]
rs10872329	1.00[ASN][1000 genomes]
rs11962214	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11965115	1.00[ASN][1000 genomes]
rs11967302	1.00[ASN][1000 genomes]
rs12110357	0.96[ASN][1000 genomes]
rs12110728	1.00[ASN][1000 genomes]
rs1339188	0.80[EUR][1000 genomes]
rs17055300	0.82[ASN][1000 genomes]
rs17055360	0.82[ASN][1000 genomes]
rs17055365	0.82[ASN][1000 genomes]
rs17055391	1.00[ASN][1000 genomes]
rs17055403	0.82[ASN][1000 genomes]
rs17055415	0.82[ASN][1000 genomes]
rs17055421	0.82[ASN][1000 genomes]
rs1738283	0.80[EUR][1000 genomes]
rs1738288	0.80[EUR][1000 genomes]
rs1738290	0.80[EUR][1000 genomes]
rs1768346	0.80[EUR][1000 genomes]
rs1856498	0.80[EUR][1000 genomes]
rs4072328	1.00[ASN][1000 genomes]
rs4440487	1.00[ASN][1000 genomes]
rs4498385	0.96[ASN][1000 genomes]
rs4895830	1.00[ASN][1000 genomes]
rs4897244	0.82[ASN][1000 genomes]
rs4897245	0.82[ASN][1000 genomes]
rs4897246	0.82[ASN][1000 genomes]
rs4897247	0.82[ASN][1000 genomes]
rs4897248	0.82[ASN][1000 genomes]
rs4897249	0.82[ASN][1000 genomes]
rs4897250	0.82[ASN][1000 genomes]
rs6904354	1.00[ASN][1000 genomes]
rs6909380	0.82[ASN][1000 genomes]
rs6918772	0.82[ASN][1000 genomes]
rs6929394	0.82[ASN][1000 genomes]
rs6929623	0.82[ASN][1000 genomes]
rs6935188	1.00[ASN][1000 genomes]
rs6938199	0.82[ASN][1000 genomes]
rs73586607	1.00[ASN][1000 genomes]
rs73586609	1.00[ASN][1000 genomes]
rs73586611	1.00[ASN][1000 genomes]
rs73586613	1.00[ASN][1000 genomes]
rs73588647	1.00[ASN][1000 genomes]
rs73590658	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7746783	0.96[ASN][1000 genomes]
rs7754321	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7768121	0.82[ASN][1000 genomes]
rs7769070	0.96[ASN][1000 genomes]
rs7772200	0.82[ASN][1000 genomes]
rs7772941	0.80[EUR][1000 genomes]
rs981998	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033443	chr6:128306654-128899203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv538440	chr6:128306654-128899203	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv604643	chr6:128359362-128493991	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv604644	chr6:128394889-128486139	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv886649	chr6:128399657-128808054	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv886650	chr6:128403745-128513395	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1031827	chr6:128418702-128497881	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv528869	chr6:128421762-128496557	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv604646	chr6:128421762-128531651	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv604647	chr6:128421762-128547177	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv886651	chr6:128450019-128565778	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv886652	chr6:128455539-128496557	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv886653	chr6:128455539-128555805	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv886654	chr6:128471938-128555805	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128450200-128480800	Weak transcription	Primary B cells from cord blood	blood
2	chr6:128452600-128505200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:128456800-128488800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:128461400-128480400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr6:128461400-128488600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:128461400-128488600	Weak transcription	NHEK	skin
7	chr6:128461400-128504400	Weak transcription	Fetal Intestine Large	intestine
8	chr6:128465600-128504400	Weak transcription	Fetal Thymus	thymus
9	chr6:128465600-128523200	Weak transcription	Left Ventricle	heart
10	chr6:128466200-128494000	Weak transcription	Fetal Heart	heart
11	chr6:128469400-128496200	Weak transcription	HepG2	liver
12	chr6:128472400-128494200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr6:128473600-128489200	Weak transcription	HMEC	breast
14	chr6:128474000-128479600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr6:128474200-128479600	Weak transcription	NH-A	brain
16	chr6:128477800-128479600	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr6:128477800-128504200	Weak transcription	HSMM	muscle
18	chr6:128479200-128480200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:128479400-128479600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:128479400-128479600	Enhancers	HUVEC	blood vessel
21	chr6:128479400-128479800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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