Variant report

Variant	rs34463732
Chromosome Location	chr6:56586013-56586014
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11961141	0.91[EUR][1000 genomes]
rs11961342	0.90[EUR][1000 genomes]
rs11968575	0.91[EUR][1000 genomes]
rs11970648	0.84[EUR][1000 genomes]
rs13192478	0.91[EUR][1000 genomes]
rs13192567	0.91[EUR][1000 genomes]
rs13198399	0.91[EUR][1000 genomes]
rs13198938	0.91[EUR][1000 genomes]
rs13203000	0.91[EUR][1000 genomes]
rs13210876	0.91[EUR][1000 genomes]
rs13213878	0.91[EUR][1000 genomes]
rs13217390	0.91[EUR][1000 genomes]
rs13219546	0.91[EUR][1000 genomes]
rs13219942	0.90[EUR][1000 genomes]
rs16888135	0.91[EUR][1000 genomes]
rs2967960	0.90[EUR][1000 genomes]
rs2967963	0.89[EUR][1000 genomes]
rs3002003	0.91[EUR][1000 genomes]
rs3002004	0.91[EUR][1000 genomes]
rs3002006	0.91[EUR][1000 genomes]
rs3002007	0.89[EUR][1000 genomes]
rs3002008	0.91[EUR][1000 genomes]
rs3002009	0.91[EUR][1000 genomes]
rs3002010	0.91[EUR][1000 genomes]
rs3002011	0.91[EUR][1000 genomes]
rs34429594	0.89[EUR][1000 genomes]
rs34455199	0.91[EUR][1000 genomes]
rs34465210	0.91[EUR][1000 genomes]
rs34566275	0.91[EUR][1000 genomes]
rs34587484	0.91[EUR][1000 genomes]
rs34623351	0.91[EUR][1000 genomes]
rs34703847	0.85[EUR][1000 genomes]
rs34803237	0.91[EUR][1000 genomes]
rs34812826	0.91[EUR][1000 genomes]
rs34824960	0.91[EUR][1000 genomes]
rs34832779	0.90[EUR][1000 genomes]
rs35326806	0.90[EUR][1000 genomes]
rs35494794	0.90[EUR][1000 genomes]
rs35876418	0.91[EUR][1000 genomes]
rs35920751	0.91[EUR][1000 genomes]
rs36068365	0.90[EUR][1000 genomes]
rs41267675	0.91[EUR][1000 genomes]
rs4275049	0.91[EUR][1000 genomes]
rs4640889	0.91[EUR][1000 genomes]
rs59085778	0.91[EUR][1000 genomes]
rs59247267	0.91[EUR][1000 genomes]
rs60498201	0.91[EUR][1000 genomes]
rs62412544	0.84[EUR][1000 genomes]
rs62412556	0.91[EUR][1000 genomes]
rs6926134	0.91[EUR][1000 genomes]
rs6938003	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491933	chr6:56177722-57171010	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv934026	chr6:56382056-57184218	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv533050	chr6:56504480-57297586	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1021651	chr6:56569444-56966319	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv538228	chr6:56569444-56966319	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56570200-56590000	Weak transcription	Right Atrium	heart
2	chr6:56579400-56592000	Weak transcription	Lung	lung
3	chr6:56580800-56592000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:56580800-56595800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr6:56581000-56589200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:56581000-56589200	Weak transcription	HSMMtube	muscle
7	chr6:56581000-56590000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr6:56581200-56587800	Weak transcription	Fetal Heart	heart
9	chr6:56581200-56589000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:56581200-56590200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:56581400-56588600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:56581400-56588600	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:56581400-56589200	Weak transcription	Brain Angular Gyrus	brain
14	chr6:56581400-56589200	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr6:56581400-56592000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:56581600-56588600	Weak transcription	Brain Substantia Nigra	brain
17	chr6:56581600-56588600	Weak transcription	Psoas Muscle	Psoas
18	chr6:56581600-56588800	Weak transcription	Brain Hippocampus Middle	brain
19	chr6:56581600-56588800	Weak transcription	NHDF-Ad	bronchial
20	chr6:56581600-56589000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:56581600-56589200	Weak transcription	NHLF	lung
22	chr6:56581600-56597800	Weak transcription	Fetal Brain Male	brain
23	chr6:56582400-56588600	Weak transcription	Brain Anterior Caudate	brain
24	chr6:56582600-56589200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr6:56582600-56589200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr6:56582600-56611600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr6:56583000-56589200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:56583600-56591200	Weak transcription	NHEK	skin
29	chr6:56583800-56590800	Weak transcription	HMEC	breast
30	chr6:56584400-56586600	Weak transcription	HSMM	muscle
31	chr6:56584400-56588400	Weak transcription	Osteobl	bone
32	chr6:56584400-56588600	Weak transcription	NH-A	brain
33	chr6:56584400-56589000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr6:56584600-56586600	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr6:56584600-56589200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr6:56584600-56593600	Weak transcription	HUVEC	blood vessel
37	chr6:56584800-56599800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:56585000-56588000	Weak transcription	Left Ventricle	heart
39	chr6:56585200-56588800	Weak transcription	HepG2	liver
40	chr6:56585600-56586200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:56585600-56586600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
42	chr6:56585800-56586200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:56586000-56587600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr6:56586000-56590000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links