Variant report

rs_ID	r²[population]
rs10828263	0.87[ASN][1000 genomes]
rs10828282	0.83[MEX][hapmap];0.90[TSI][hapmap]
rs12358164	0.84[MEX][hapmap]
rs1891393	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2068357	0.83[MEX][hapmap];0.92[TSI][hapmap]
rs2840320	0.83[ASW][hapmap]
rs61084330	0.95[ASN][1000 genomes]
rs7900124	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18424200-18428800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:18425000-18428600	Weak transcription	Colon Smooth Muscle	Colon
3	chr10:18425000-18428600	Weak transcription	Fetal Heart	heart
4	chr10:18425200-18428600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr10:18425600-18428800	Weak transcription	Brain Anterior Caudate	brain
6	chr10:18425800-18428600	Weak transcription	Brain Substantia Nigra	brain
7	chr10:18425800-18429000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:18426000-18428600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr10:18428200-18428600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr10:18428200-18428800	Active TSS	Primary hematopoietic stem cells	blood
11	chr10:18428400-18428600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:18428400-18428600	Enhancers	Stomach Smooth Muscle	stomach
13	chr10:18428400-18428800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr10:18428400-18428800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr10:18428400-18428800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr10:18428400-18428800	Enhancers	Aorta	Aorta
17	chr10:18428400-18429200	Bivalent Enhancer	Fetal Brain Male	brain

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