Variant report

Variant	rs1225076
Chromosome Location	chr2:190614034-190614035
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:190613440..190615981-chr2:190627652..190629177,2	K562	blood:
2	chr2:190612378..190614940-chr2:190626343..190629177,2	K562	blood:
3	chr2:190612390..190614561-chr2:190647574..190650409,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128694	Chromatin interaction
ENSG00000128699	Chromatin interaction
ENSG00000064933	Chromatin interaction
ENSG00000253559	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11883813	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11888192	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1225083	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1225097	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1225100	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1225105	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1225111	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1225119	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1225121	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1470100	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1898559	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2066459	1.00[CHD][hapmap]
rs2196670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4667301	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5742925	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5742934	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6434362	1.00[AMR][1000 genomes]
rs6708086	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6736443	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:190540800-190618400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr2:190541600-190617000	Weak transcription	Colon Smooth Muscle	Colon
3	chr2:190550800-190617000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:190550800-190626800	Weak transcription	Right Ventricle	heart
5	chr2:190551200-190617000	Weak transcription	HSMM	muscle
6	chr2:190557400-190617000	Weak transcription	Brain Angular Gyrus	brain
7	chr2:190575000-190615800	Weak transcription	Fetal Kidney	kidney
8	chr2:190576800-190627000	Weak transcription	Pancreas	Pancrea
9	chr2:190577000-190622600	Weak transcription	Aorta	Aorta
10	chr2:190583000-190626800	Weak transcription	Psoas Muscle	Psoas
11	chr2:190589400-190626600	Weak transcription	HUVEC	blood vessel
12	chr2:190590800-190614800	Weak transcription	Esophagus	oesophagus
13	chr2:190594800-190627000	Weak transcription	Gastric	stomach
14	chr2:190597800-190626600	Weak transcription	Fetal Heart	heart
15	chr2:190599000-190626800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr2:190600800-190616600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:190601400-190626800	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr2:190602400-190617000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr2:190602400-190626400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr2:190603800-190626800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:190605000-190626800	Weak transcription	Fetal Brain Male	brain
22	chr2:190607000-190619200	Weak transcription	NHDF-Ad	bronchial
23	chr2:190607000-190626800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr2:190607000-190626800	Weak transcription	NH-A	brain
25	chr2:190607400-190626800	Weak transcription	HSMMtube	muscle
26	chr2:190607800-190621000	Strong transcription	Liver	Liver
27	chr2:190607800-190622400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr2:190608400-190620200	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr2:190608600-190614400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr2:190608600-190626200	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr2:190608800-190614200	Strong transcription	Primary B cells from peripheral blood	blood
32	chr2:190609000-190614600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr2:190609400-190617400	Weak transcription	Brain Anterior Caudate	brain
34	chr2:190609600-190626600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr2:190609600-190627000	Weak transcription	Small Intestine	intestine
36	chr2:190609800-190614200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:190609800-190620400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:190609800-190626200	Weak transcription	HMEC	breast
39	chr2:190610000-190614800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr2:190610000-190615000	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr2:190610000-190626800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr2:190610200-190616800	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr2:190610200-190627000	Weak transcription	Lung	lung
44	chr2:190610200-190627000	Weak transcription	Spleen	Spleen
45	chr2:190610400-190626200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr2:190610400-190626800	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr2:190610400-190626800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr2:190610400-190627000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr2:190610800-190617000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr2:190610800-190617800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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