Variant report

rs_ID	r²[population]
rs10918893	1.00[ASN][1000 genomes]
rs10918895	0.89[ASN][1000 genomes]
rs10918896	0.89[ASN][1000 genomes]
rs12062332	0.83[ASN][1000 genomes]
rs12069559	1.00[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12069600	0.89[ASN][1000 genomes]
rs12071580	0.89[ASN][1000 genomes]
rs12071946	0.89[ASN][1000 genomes]
rs12072186	1.00[AMR][1000 genomes]
rs12075499	1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12094971	0.83[AMR][1000 genomes]
rs12563551	1.00[CHB][hapmap];0.95[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs12564897	1.00[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2056963	1.00[YRI][hapmap]
rs74120912	1.00[ASN][1000 genomes]
rs74120913	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168422800-168426200	Enhancers	NHDF-Ad	bronchial
2	chr1:168423000-168426200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:168423000-168426200	Enhancers	HSMMtube	muscle
4	chr1:168423000-168426600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:168423000-168426600	Enhancers	HMEC	breast
6	chr1:168423000-168430600	Weak transcription	Liver	Liver
7	chr1:168423400-168426400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:168423400-168427200	Enhancers	NHEK	skin
9	chr1:168424800-168426400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:168425200-168426200	Enhancers	Colon Smooth Muscle	Colon
11	chr1:168425200-168426600	Enhancers	Placenta Amnion	Placenta Amnion
12	chr1:168425400-168426200	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr1:168425600-168426200	Enhancers	Fetal Heart	heart
14	chr1:168426000-168435200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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