Variant report

Variant	rs9292869
Chromosome Location	chr5:43292808-43292809
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:43286983..43288744-chr5:43291161..43294149,3	K562	blood:
2	chr5:43284931..43287832-chr5:43292804..43295687,2	MCF-7	breast:
3	chr5:43290130..43293263-chr5:43311946..43314740,3	MCF-7	breast:
4	chr5:43286983..43288744-chr5:43291161..43294149,2	K562	blood:

Variant related genes	Relation type
ENSG00000261604	Chromatin interaction
ENSG00000112972	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10037409	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10037706	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap]
rs10038859	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10040897	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs10043148	1.00[CEU][hapmap];0.83[YRI][hapmap];0.86[EUR][1000 genomes]
rs10052384	0.86[EUR][1000 genomes]
rs10054415	1.00[CEU][hapmap];0.84[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10056437	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs10062031	0.86[EUR][1000 genomes]
rs10062121	0.86[EUR][1000 genomes]
rs10062598	1.00[CEU][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10064967	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10067763	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10069507	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap]
rs10077324	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10079530	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10473306	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10473308	1.00[CEU][hapmap];0.84[YRI][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11955467	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1478436	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16874093	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16874094	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28450849	0.86[EUR][1000 genomes]
rs28608156	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28688522	0.85[AMR][1000 genomes]
rs28856961	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4326149	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55645370	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60520238	1.00[EUR][1000 genomes]
rs6865440	1.00[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.82[YRI][hapmap];0.86[EUR][1000 genomes]
rs6884349	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6887169	1.00[MEX][hapmap]
rs6892413	0.86[EUR][1000 genomes]
rs6893898	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6894240	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs6895237	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap]
rs7356654	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7356727	0.87[AMR][1000 genomes]
rs73751075	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73751078	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73751082	0.86[EUR][1000 genomes]
rs73751083	0.86[EUR][1000 genomes]
rs7710717	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7715267	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7729140	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7729145	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7733732	1.00[CEU][hapmap];0.82[YRI][hapmap];0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9292870	1.00[CEU][hapmap];1.00[GIH][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.88[YRI][hapmap];0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9292872	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9292875	1.00[CEU][hapmap];0.84[YRI][hapmap];0.87[AMR][1000 genomes];0.86[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	nsv1023741	chr5:42768215-43348145	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
2	nsv537737	chr5:42768215-43348145	Genic enhancers Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription 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	309 gene(s)	inside rSNPs	diseases
3	nsv1024636	chr5:42959979-43295782	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
4	nsv537739	chr5:42959979-43295782	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
5	nsv508352	chr5:43237830-43391062	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43284200-43294000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:43284200-43309400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:43285000-43293400	Weak transcription	Pancreas	Pancrea
4	chr5:43285000-43300800	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr5:43285200-43294200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr5:43285600-43293400	Weak transcription	Colonic Mucosa	Colon
7	chr5:43285600-43300000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr5:43285600-43302000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr5:43285600-43302800	Strong transcription	Duodenum Mucosa	Duodenum
10	chr5:43286200-43295600	Strong transcription	HSMMtube	muscle
11	chr5:43286200-43298000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:43286200-43300600	Strong transcription	Fetal Intestine Large	intestine
13	chr5:43286400-43302200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:43286400-43302400	Strong transcription	GM12878-XiMat	blood
15	chr5:43286600-43293200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr5:43286600-43293200	Strong transcription	Brain Substantia Nigra	brain
17	chr5:43286600-43296400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:43286600-43300400	Strong transcription	Fetal Thymus	thymus
19	chr5:43286600-43300800	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr5:43286600-43301000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr5:43286600-43301400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr5:43286600-43303000	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr5:43286600-43303000	Strong transcription	Primary hematopoietic stem cells	blood
24	chr5:43286800-43294200	Strong transcription	NHDF-Ad	bronchial
25	chr5:43286800-43294400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:43286800-43294600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:43286800-43294600	Strong transcription	Fetal Muscle Trunk	muscle
28	chr5:43286800-43297000	Strong transcription	Liver	Liver
29	chr5:43286800-43297400	Strong transcription	Dnd41	blood
30	chr5:43286800-43300000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr5:43286800-43300400	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr5:43286800-43300400	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr5:43286800-43301000	Strong transcription	K562	blood
34	chr5:43286800-43301400	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr5:43286800-43301800	Strong transcription	HMEC	breast
36	chr5:43286800-43302400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr5:43286800-43302600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:43286800-43302600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr5:43286800-43304400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr5:43287000-43302800	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr5:43287000-43305000	Strong transcription	HUVEC	blood vessel
42	chr5:43287200-43301000	Strong transcription	Primary B cells from peripheral blood	blood
43	chr5:43287400-43298600	Weak transcription	Right Ventricle	heart
44	chr5:43287400-43300800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr5:43287400-43302600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr5:43287400-43302800	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:43287600-43295800	Strong transcription	NHEK	skin
48	chr5:43287600-43302000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:43287800-43298800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:43287800-43299400	Strong transcription	H1 Cell Line	embryonic stem cell

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