Variant report

Variant	rs4646383
Chromosome Location	chr17:17454883-17454884
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:17449610..17452428-chr17:17454870..17458943,3	MCF-7	breast:
2	chr17:17444761..17447453-chr17:17453663..17455413,2	K562	blood:
3	chr17:17451529..17456162-chr17:17456259..17460340,5	K562	blood:
4	chr17:17453470..17455947-chr17:17461271..17462864,2	MCF-7	breast:
5	chr17:17398601..17400670-chr17:17453497..17457003,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000108551	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1020697	1.00[CEU][hapmap]
rs2278952	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3744117	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3760187	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4646348	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4646367	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4646379	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4646380	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4646381	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4646398	1.00[CEU][hapmap]
rs4646400	1.00[CEU][hapmap]
rs56656484	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57417963	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58146226	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58356850	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58810148	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58956930	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60343188	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs70959694	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8075019	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482648	chr17:17315268-17455442	Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv907731	chr17:17358004-17504856	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription 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	25 gene(s)	inside rSNPs	diseases
3	nsv907736	chr17:17381764-17465458	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv907744	chr17:17404586-17504856	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv907746	chr17:17412032-17478917	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv907747	chr17:17412032-17504856	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv907748	chr17:17412032-17782404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
8	nsv470579	chr17:17424332-17493810	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv1065270	chr17:17430116-17823086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
10	nsv543236	chr17:17430116-17823086	Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
11	nsv907750	chr17:17439458-17460180	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17418200-17478000	Weak transcription	Primary T cells from cord blood	blood
2	chr17:17424600-17460000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr17:17436800-17479200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr17:17442800-17456400	Weak transcription	Small Intestine	intestine
5	chr17:17443400-17467000	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr17:17444200-17467400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr17:17444400-17469200	Weak transcription	Fetal Brain Female	brain
8	chr17:17444600-17460400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr17:17444600-17464600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr17:17444800-17464000	Weak transcription	Esophagus	oesophagus
11	chr17:17445200-17468400	Weak transcription	Thymus	Thymus
12	chr17:17445200-17473200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr17:17447400-17461000	Weak transcription	Pancreas	Pancrea
14	chr17:17449000-17459000	Weak transcription	Spleen	Spleen
15	chr17:17449000-17464800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr17:17449600-17464800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr17:17449600-17467000	Weak transcription	Ovary	ovary
18	chr17:17450800-17467800	Weak transcription	Brain Germinal Matrix	brain
19	chr17:17451000-17455400	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr17:17451000-17468400	Weak transcription	Stomach Smooth Muscle	stomach
21	chr17:17451400-17461200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr17:17451600-17455000	Weak transcription	Right Atrium	heart
23	chr17:17453000-17455200	Enhancers	Fetal Intestine Large	intestine
24	chr17:17453200-17455000	Enhancers	Brain Hippocampus Middle	brain
25	chr17:17453200-17455000	Enhancers	Brain Substantia Nigra	brain
26	chr17:17453200-17456000	Enhancers	Liver	Liver
27	chr17:17453200-17457400	Enhancers	Left Ventricle	heart
28	chr17:17453200-17468200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr17:17453400-17477800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr17:17453600-17457000	Enhancers	Right Ventricle	heart
31	chr17:17453800-17455200	Enhancers	HepG2	liver
32	chr17:17453800-17456600	Enhancers	Fetal Muscle Leg	muscle
33	chr17:17454000-17455200	Enhancers	Duodenum Mucosa	Duodenum
34	chr17:17454000-17455200	Enhancers	Stomach Mucosa	stomach
35	chr17:17454000-17455400	Enhancers	Fetal Intestine Small	intestine
36	chr17:17454000-17455400	Enhancers	Fetal Stomach	stomach
37	chr17:17454000-17456200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr17:17454200-17455200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr17:17454200-17455200	Enhancers	Adipose Nuclei	Adipose
40	chr17:17454200-17455200	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr17:17454200-17455200	Enhancers	Fetal Kidney	kidney
42	chr17:17454200-17455200	Enhancers	Fetal Lung	lung
43	chr17:17454400-17455000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr17:17454400-17455000	Enhancers	Fetal Brain Male	brain
45	chr17:17454400-17455200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr17:17454400-17455200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr17:17454400-17455200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr17:17454400-17455200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr17:17454400-17455200	Enhancers	Placenta	Placenta
50	chr17:17454400-17455800	Enhancers	Skeletal Muscle Male	skeletal muscle

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