Variant report

rs_ID	r²[population]
rs10945183	0.83[EUR][1000 genomes]
rs13206442	0.86[EUR][1000 genomes]
rs310267	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs310268	0.83[EUR][1000 genomes]
rs310269	0.83[EUR][1000 genomes]
rs7762919	0.82[EUR][1000 genomes]
rs9346313	0.82[EUR][1000 genomes]
rs9360392	0.81[EUR][1000 genomes]
rs9446142	0.82[EUR][1000 genomes]

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70289000-70294400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr6:70289000-70294400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr6:70291600-70294400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr6:70291800-70294800	Weak transcription	Fetal Brain Male	brain
5	chr6:70292200-70294400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:70292800-70296200	Enhancers	HSMM	muscle
7	chr6:70293400-70294400	Enhancers	Fetal Heart	heart
8	chr6:70293600-70295800	Enhancers	HSMMtube	muscle
9	chr6:70293800-70295600	Enhancers	Colon Smooth Muscle	Colon
10	chr6:70294200-70295000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr6:70294200-70295400	Enhancers	Primary hematopoietic stem cells	blood
12	chr6:70294200-70296200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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