Variant report

Variant	rs73539675
Chromosome Location	chr6:132176309-132176310
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12660595	1.00[AMR][1000 genomes]
rs12661063	1.00[AMR][1000 genomes]
rs12662953	1.00[AMR][1000 genomes]
rs12663389	1.00[AMR][1000 genomes]
rs12664747	1.00[AMR][1000 genomes]
rs12664750	1.00[AMR][1000 genomes]
rs12665617	1.00[AMR][1000 genomes]
rs3908474	1.00[AMR][1000 genomes]
rs4371863	1.00[AMR][1000 genomes]
rs61027777	1.00[AMR][1000 genomes]
rs73537697	1.00[AMR][1000 genomes]
rs73539605	1.00[AMR][1000 genomes]
rs73539606	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv515476	chr6:131615425-132228577	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv7968	chr6:131917172-132321099	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv886670	chr6:132071193-132193395	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
4	nsv886671	chr6:132071193-132203432	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 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	chr6:132147600-132199200	Weak transcription	Fetal Stomach	stomach
2	chr6:132151600-132182400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:132159600-132179800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr6:132160000-132180600	Weak transcription	Placenta	Placenta
5	chr6:132162200-132211000	Weak transcription	Fetal Kidney	kidney
6	chr6:132162600-132181000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:132163000-132181000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:132163000-132182600	Weak transcription	HSMMtube	muscle
9	chr6:132163000-132213600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:132163400-132179200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:132163600-132183400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr6:132166000-132180000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:132166000-132185000	Weak transcription	Fetal Intestine Large	intestine
14	chr6:132166200-132179800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:132168000-132179200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:132168800-132183800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr6:132169800-132181000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr6:132170600-132201800	Weak transcription	Left Ventricle	heart
19	chr6:132170800-132211200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr6:132171000-132180200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:132171200-132183800	Weak transcription	Stomach Mucosa	stomach
22	chr6:132171200-132209400	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr6:132172400-132180000	Weak transcription	HSMM	muscle
24	chr6:132172400-132184600	Weak transcription	Fetal Muscle Leg	muscle
25	chr6:132172400-132196800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr6:132172600-132180800	Weak transcription	Aorta	Aorta
27	chr6:132172600-132184600	Weak transcription	Fetal Intestine Small	intestine
28	chr6:132172800-132198200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:132173000-132192600	Weak transcription	Adipose Nuclei	Adipose
30	chr6:132173200-132176600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr6:132173200-132181000	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr6:132173800-132179200	Weak transcription	NHLF	lung
33	chr6:132175600-132176600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:132175800-132176400	Genic enhancers	Liver	Liver
35	chr6:132175800-132176800	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr6:132176000-132176400	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr6:132176000-132176400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:132176000-132176400	Strong transcription	NH-A	brain
39	chr6:132176000-132176400	Genic enhancers	Osteobl	bone
40	chr6:132176000-132176800	Strong transcription	Fetal Muscle Trunk	muscle
41	chr6:132176000-132177000	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr6:132176000-132177000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr6:132176200-132177400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr6:132176200-132177400	Strong transcription	HepG2	liver

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