Variant report

Variant	rs73275997
Chromosome Location	chr10:44373377-44373378
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs2298204	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56942692	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57645083	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57882812	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58526299	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58838440	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59084049	0.93[EUR][1000 genomes]
rs59274145	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59658376	0.82[ASN][1000 genomes]
rs59668941	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59834212	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59983288	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60606176	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60833858	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60927183	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61110542	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61525746	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs713496	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73275973	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73275981	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73275989	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73275990	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73275995	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73275998	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74138916	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44360000-44392200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:44364200-44374000	Weak transcription	NHLF	lung
3	chr10:44365000-44373400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr10:44365000-44373400	Weak transcription	Right Ventricle	heart
5	chr10:44367400-44373600	Weak transcription	Fetal Stomach	stomach
6	chr10:44368400-44373600	Weak transcription	Brain Cingulate Gyrus	brain
7	chr10:44368400-44377200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr10:44371400-44375200	Enhancers	Fetal Kidney	kidney
9	chr10:44371800-44373600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr10:44373000-44374800	Enhancers	Fetal Heart	heart
11	chr10:44373200-44373800	Enhancers	Spleen	Spleen
12	chr10:44373200-44374000	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr10:44373200-44374400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr10:44373200-44374600	Enhancers	Fetal Lung	lung
15	chr10:44373200-44375800	Enhancers	Muscle Satellite Cultured Cells	--
16	chr10:44373200-44375800	Enhancers	Left Ventricle	heart
17	chr10:44373200-44375800	Enhancers	Right Atrium	heart
18	chr10:44373200-44376000	Enhancers	NHDF-Ad	bronchial
19	chr10:44373200-44376200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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