Variant report

Variant	rs9296152
Chromosome Location	chr6:35379973-35379974
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:35379744..35382549-chr6:35384456..35386159,2	K562	blood:
2	chr6:35311343..35313343-chr6:35379052..35381672,2	MCF-7	breast:
3	chr6:35374379..35377300-chr6:35379343..35382186,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1053046	0.89[ASN][1000 genomes]
rs57648364	0.89[ASN][1000 genomes]
rs59137976	0.89[ASN][1000 genomes]
rs60987797	0.95[ASN][1000 genomes]
rs6906237	0.95[ASN][1000 genomes]
rs73413756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7749664	0.89[ASN][1000 genomes]
rs9296151	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9296153	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9296154	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9462081	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9470023	0.86[EUR][1000 genomes]
rs9658151	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830641	chr6:35282534-35440603	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
2	nsv462907	chr6:35333799-35408959	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv602908	chr6:35333799-35408959	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv602909	chr6:35356640-35423489	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv470812	chr6:35374461-35418118	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv528351	chr6:35377922-35465786	Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
7	nsv885799	chr6:35378778-35442397	Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
8	nsv462908	chr6:35378778-35457396	Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
9	nsv602910	chr6:35378778-35457396	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
10	nsv519370	chr6:35378778-35537406	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	72 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35360000-35382600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:35361800-35385800	Weak transcription	Small Intestine	intestine
3	chr6:35362200-35380000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:35366200-35386800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr6:35366400-35382800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr6:35369200-35382600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:35369400-35382600	Weak transcription	NH-A	brain
8	chr6:35370600-35393200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:35371000-35382400	Weak transcription	Right Atrium	heart
10	chr6:35371200-35382400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr6:35371200-35382400	Weak transcription	Stomach Mucosa	stomach
12	chr6:35371200-35383200	Weak transcription	Fetal Kidney	kidney
13	chr6:35372000-35382400	Weak transcription	Fetal Heart	heart
14	chr6:35373200-35381400	Weak transcription	Fetal Brain Male	brain
15	chr6:35373400-35382400	Weak transcription	Brain Germinal Matrix	brain
16	chr6:35374000-35380400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:35375200-35382600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr6:35375600-35387000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr6:35376000-35380000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr6:35377600-35380200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:35377600-35381200	Strong transcription	Liver	Liver
22	chr6:35377600-35382400	Strong transcription	Fetal Muscle Leg	muscle
23	chr6:35377600-35382400	Strong transcription	Osteobl	bone
24	chr6:35377600-35386000	Weak transcription	HUVEC	blood vessel
25	chr6:35377800-35385600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr6:35377800-35395000	Weak transcription	K562	blood
27	chr6:35378000-35380000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
28	chr6:35378000-35380400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:35378000-35381200	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr6:35378000-35381200	Strong transcription	Skeletal Muscle Female	skeletal muscle
31	chr6:35378000-35381400	Strong transcription	Gastric	stomach
32	chr6:35378000-35381400	Strong transcription	Rectal Mucosa Donor 29	rectum
33	chr6:35378000-35381800	Strong transcription	Stomach Smooth Muscle	stomach
34	chr6:35378000-35382400	Strong transcription	Fetal Stomach	stomach
35	chr6:35378000-35382600	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr6:35378000-35386400	Strong transcription	Spleen	Spleen
37	chr6:35378200-35381000	Strong transcription	Colon Smooth Muscle	Colon
38	chr6:35378200-35381000	Strong transcription	Lung	lung
39	chr6:35378200-35381200	Strong transcription	Brain Cingulate Gyrus	brain
40	chr6:35378200-35381800	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr6:35378200-35382400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr6:35378200-35382400	Strong transcription	Esophagus	oesophagus
43	chr6:35378200-35382800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr6:35378400-35380400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr6:35378400-35380800	Strong transcription	Aorta	Aorta
46	chr6:35378400-35381400	Strong transcription	HSMMtube	muscle
47	chr6:35378400-35381800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:35378400-35381800	Strong transcription	Brain Anterior Caudate	brain
49	chr6:35378400-35381800	Strong transcription	Brain Hippocampus Middle	brain
50	chr6:35378400-35382000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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