Variant report

Variant	rs9559656
Chromosome Location	chr13:110429444-110429445
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11841502	0.87[CHB][hapmap];0.91[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12853546	0.91[ASN][1000 genomes]
rs12864020	0.90[ASN][1000 genomes]
rs12874640	0.90[ASN][1000 genomes]
rs12876234	0.81[CEU][hapmap];0.88[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs1414317	0.90[ASN][1000 genomes]
rs1967852	0.80[ASN][1000 genomes]
rs1974134	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34701391	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34911155	0.90[ASN][1000 genomes]
rs35887251	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4372569	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4771645	0.81[CEU][hapmap];0.88[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs4771646	0.81[CEU][hapmap];0.88[CHB][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4771647	0.87[CHB][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4773088	0.83[JPT][hapmap]
rs4773091	0.81[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4773093	0.90[ASN][1000 genomes]
rs4773094	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs55824992	0.90[ASN][1000 genomes]
rs56920445	0.88[ASN][1000 genomes]
rs9555633	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9555635	0.90[ASN][1000 genomes]
rs9559648	0.83[JPT][hapmap]
rs9559650	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9559654	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9559657	0.90[ASN][1000 genomes]
rs9559658	0.88[ASN][1000 genomes]
rs9559659	0.90[ASN][1000 genomes]
rs9559660	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv826788	chr13:110381750-110469062	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv826789	chr13:110387268-110473524	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv826790	chr13:110395165-110463032	Weak transcription Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv826791	chr13:110397733-110462553	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv826792	chr13:110398678-110462209	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	nsv1047427	chr13:110412864-110446417	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv826793	chr13:110423187-110448628	Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
8	nsv826794	chr13:110424916-110448628	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	n/a
9	nsv826795	chr13:110425465-110448628	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110397200-110430400	Weak transcription	NHLF	lung
2	chr13:110401800-110430800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr13:110403200-110430600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr13:110408600-110430400	Weak transcription	Colonic Mucosa	Colon
5	chr13:110409000-110431200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:110409400-110429800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr13:110409400-110430200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr13:110413400-110430400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr13:110413600-110430800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr13:110416000-110430800	Weak transcription	Fetal Kidney	kidney
11	chr13:110417000-110432400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr13:110417200-110430400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr13:110417200-110431600	Weak transcription	Fetal Muscle Leg	muscle
14	chr13:110417400-110430200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr13:110417600-110430400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:110417600-110430400	Weak transcription	Thymus	Thymus
17	chr13:110417600-110430600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr13:110417800-110430200	Weak transcription	Fetal Thymus	thymus
19	chr13:110419600-110429600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr13:110423000-110433400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr13:110423200-110430200	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr13:110423200-110430400	Weak transcription	NHDF-Ad	bronchial
23	chr13:110423200-110433200	Weak transcription	Gastric	stomach
24	chr13:110423600-110431000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr13:110424200-110430000	Weak transcription	Duodenum Mucosa	Duodenum
26	chr13:110424800-110430200	Weak transcription	Fetal Intestine Large	intestine
27	chr13:110424800-110430800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr13:110424800-110431000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr13:110424800-110433200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr13:110425000-110429600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr13:110425000-110429800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr13:110425000-110430000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr13:110425000-110430200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr13:110425000-110430200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr13:110425000-110430200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr13:110425000-110430200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr13:110425000-110430600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr13:110425000-110430800	Weak transcription	Lung	lung
39	chr13:110425000-110431000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr13:110425000-110431400	Weak transcription	Placenta	Placenta
41	chr13:110425000-110432000	Weak transcription	Fetal Stomach	stomach
42	chr13:110425000-110433400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr13:110425000-110433400	Weak transcription	Esophagus	oesophagus
44	chr13:110425000-110433400	Weak transcription	Pancreas	Pancrea
45	chr13:110425000-110433400	Weak transcription	Spleen	Spleen
46	chr13:110425400-110432600	Weak transcription	Fetal Intestine Small	intestine
47	chr13:110425800-110430200	Enhancers	Brain Substantia Nigra	brain
48	chr13:110426000-110430600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr13:110426800-110430200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr13:110427600-110430600	Enhancers	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links