Variant report

Variant	rs4656783
Chromosome Location	chr1:170516078-170516079
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:170499846..170504184-chr1:170513564..170517681,4	K562	blood:
2	chr1:170499494..170507345-chr1:170507805..170517333,18	K562	blood:

Variant related genes	Relation type
ENSG00000231407	Chromatin interaction
ENSG00000120370	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10157476	0.81[AFR][1000 genomes]
rs10733056	0.89[AFR][1000 genomes]
rs10753814	0.88[AFR][1000 genomes]
rs10753815	0.90[AFR][1000 genomes]
rs10800527	0.97[AFR][1000 genomes]
rs10919425	0.89[AFR][1000 genomes]
rs12116909	0.89[AFR][1000 genomes]
rs1333133	0.89[AFR][1000 genomes]
rs1333150	0.93[AFR][1000 genomes]
rs1333152	0.81[AFR][1000 genomes]
rs1333155	0.91[AFR][1000 genomes]
rs1333156	0.91[AFR][1000 genomes]
rs1412892	0.97[AFR][1000 genomes]
rs1412893	0.97[AFR][1000 genomes]
rs1412894	0.81[AFR][1000 genomes]
rs1412895	0.91[AFR][1000 genomes]
rs1537397	0.88[AFR][1000 genomes]
rs1576979	0.86[AFR][1000 genomes]
rs1576980	0.89[AFR][1000 genomes]
rs1855221	0.91[AFR][1000 genomes]
rs1930632	0.81[AFR][1000 genomes]
rs2104918	0.88[AFR][1000 genomes]
rs2150029	0.86[AFR][1000 genomes]
rs2225322	0.88[AFR][1000 genomes]
rs2421325	0.97[AFR][1000 genomes]
rs2901401	0.89[AFR][1000 genomes]
rs3980839	0.93[AFR][1000 genomes]
rs4233350	0.83[AFR][1000 genomes]
rs4325194	0.91[AFR][1000 genomes]
rs4402174	0.87[AFR][1000 genomes]
rs4415629	0.91[AFR][1000 genomes]
rs4656769	0.86[AFR][1000 genomes]
rs4656775	0.89[AFR][1000 genomes]
rs4656777	0.89[AFR][1000 genomes]
rs4656779	0.89[AFR][1000 genomes]
rs6427260	0.97[AFR][1000 genomes]
rs6427261	0.97[AFR][1000 genomes]
rs6657164	0.87[AFR][1000 genomes]
rs6660575	0.90[AFR][1000 genomes]
rs6664037	0.93[AFR][1000 genomes]
rs6667304	0.94[AFR][1000 genomes]
rs6669308	0.97[AFR][1000 genomes]
rs6670724	0.89[AFR][1000 genomes]
rs6671312	0.97[AFR][1000 genomes]
rs6676081	0.92[AFR][1000 genomes]
rs6693763	0.97[AFR][1000 genomes]
rs6699057	0.86[AFR][1000 genomes]
rs6701218	0.92[AFR][1000 genomes]
rs6703801	0.83[AFR][1000 genomes]
rs7523665	0.84[AFR][1000 genomes]
rs7531125	0.90[AFR][1000 genomes]
rs7538125	0.91[AFR][1000 genomes]
rs7548443	0.87[AFR][1000 genomes]
rs7553254	0.95[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872543	chr1:170171083-170674903	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv533915	chr1:170258766-170725296	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170502000-170517200	Weak transcription	Esophagus	oesophagus
2	chr1:170502200-170521000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:170502600-170520800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr1:170502600-170523400	Weak transcription	Fetal Brain Male	brain
5	chr1:170503000-170516400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:170503000-170523600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr1:170505000-170524800	Strong transcription	Dnd41	blood
8	chr1:170505400-170522800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:170506000-170522200	Strong transcription	Primary B cells from cord blood	blood
10	chr1:170506600-170516800	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr1:170506600-170519200	Weak transcription	Gastric	stomach
12	chr1:170506600-170519200	Weak transcription	Right Ventricle	heart
13	chr1:170507400-170516400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:170507400-170516400	Weak transcription	HSMMtube	muscle
15	chr1:170507600-170516200	Weak transcription	Stomach Mucosa	stomach
16	chr1:170507600-170523600	Strong transcription	Primary B cells from peripheral blood	blood
17	chr1:170507600-170524000	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr1:170507800-170516400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:170507800-170521800	Strong transcription	Fetal Lung	lung
20	chr1:170507800-170522200	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr1:170507800-170522600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
22	chr1:170508000-170516400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:170508000-170522000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:170508000-170523000	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr1:170508200-170516400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr1:170508200-170522200	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr1:170508200-170523400	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr1:170508200-170524400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:170508400-170516400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr1:170508400-170519600	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr1:170508400-170521600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr1:170508400-170522000	Strong transcription	Placenta	Placenta
33	chr1:170508400-170522200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
34	chr1:170508400-170522200	Strong transcription	Primary hematopoietic stem cells	blood
35	chr1:170508400-170522200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr1:170508400-170522200	Strong transcription	Duodenum Mucosa	Duodenum
37	chr1:170508400-170522200	Strong transcription	Fetal Thymus	thymus
38	chr1:170508400-170522200	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr1:170508400-170522400	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr1:170508400-170523600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr1:170508400-170523600	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr1:170508400-170523800	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr1:170508400-170523800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr1:170508800-170524000	Strong transcription	Liver	Liver
45	chr1:170509200-170522200	Strong transcription	Primary T cells from cord blood	blood
46	chr1:170509600-170522200	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr1:170509800-170523600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr1:170510200-170517800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
49	chr1:170510800-170516400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:170512000-170522200	Strong transcription	A549	lung

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