Variant report

Variant	rs4946732
Chromosome Location	chr6:106629035-106629036
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	chr6:106622833..106624586-chr6:106626534..106629325,2	MCF-7	breast:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12197000	0.82[ASN][1000 genomes]
rs12212377	0.82[ASN][1000 genomes]
rs1475270	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1951485	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2284193	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2743559	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs473543	0.83[ASN][1000 genomes]
rs484621	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs490010	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs506027	0.83[ASN][1000 genomes]
rs510432	0.83[ASN][1000 genomes]
rs524428	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs532906	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs546456	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs547738	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs579801	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs594819	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs597443	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs617994	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs644232	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs665791	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs669975	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs698029	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs803360	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs803362	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932155	chr6:106281728-107030467	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv1025231	chr6:106451012-106634389	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1025900	chr6:106529777-106898421	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv1018270	chr6:106531658-106908606	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv538399	chr6:106531658-106908606	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	esv1832544	chr6:106539914-106642993	Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv1035110	chr6:106557281-106802212	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
8	nsv538400	chr6:106557281-106802212	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv1022855	chr6:106570926-106802072	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
10	nsv538401	chr6:106570926-106802072	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
11	nsv1019265	chr6:106587627-106727591	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv538402	chr6:106587627-106727591	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers 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
13	nsv532047	chr6:106591482-107143252	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
14	nsv1025963	chr6:106593639-106848778	Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
15	nsv1020047	chr6:106597828-106912047	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106612400-106662000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:106613200-106633400	Weak transcription	Primary B cells from cord blood	blood
3	chr6:106614200-106629800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:106616200-106629800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:106616400-106654200	Weak transcription	Aorta	Aorta
6	chr6:106617000-106629400	Weak transcription	HSMM	muscle
7	chr6:106623600-106633400	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr6:106624600-106629200	Weak transcription	HSMMtube	muscle
9	chr6:106625600-106638400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr6:106625600-106642000	Weak transcription	Small Intestine	intestine
11	chr6:106625800-106648400	Weak transcription	Fetal Muscle Leg	muscle
12	chr6:106625800-106651800	Weak transcription	Esophagus	oesophagus
13	chr6:106625800-106652800	Weak transcription	Brain Germinal Matrix	brain
14	chr6:106626000-106629200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:106626000-106629200	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr6:106626000-106629200	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr6:106626000-106629200	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr6:106626000-106629400	Weak transcription	NHEK	skin
19	chr6:106626000-106633600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:106626000-106637600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr6:106626200-106629200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr6:106626200-106630200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr6:106626400-106629400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:106626400-106629400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:106626400-106629800	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr6:106626600-106629200	Enhancers	GM12878-XiMat	blood
27	chr6:106626600-106645000	Weak transcription	Fetal Heart	heart
28	chr6:106626800-106633600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr6:106626800-106674800	Weak transcription	K562	blood
30	chr6:106627000-106633800	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr6:106627200-106634000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:106627200-106634000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:106627200-106643600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr6:106627400-106629200	Enhancers	Colonic Mucosa	Colon
35	chr6:106627600-106629200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr6:106628000-106659200	Weak transcription	HepG2	liver
37	chr6:106628200-106634200	Weak transcription	Dnd41	blood
38	chr6:106628400-106642000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:106628400-106675200	Weak transcription	Stomach Mucosa	stomach
40	chr6:106628600-106633200	Weak transcription	Primary T cells from cord blood	blood
41	chr6:106628600-106647800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr6:106628800-106633600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr6:106628800-106634000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr6:106628800-106648000	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr6:106628800-106671200	Weak transcription	Fetal Intestine Small	intestine
46	chr6:106629000-106629200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr6:106629000-106631000	Enhancers	Osteobl	bone
48	chr6:106629000-106634000	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr6:106629000-106634000	Weak transcription	Fetal Intestine Large	intestine

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