Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1379309	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1379310	0.81[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs1457132	0.93[ASN][1000 genomes]
rs1565968	0.84[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs172753	0.90[ASN][1000 genomes]
rs2124942	0.96[ASN][1000 genomes]
rs2124943	0.96[ASN][1000 genomes]
rs2445888	0.86[ASN][1000 genomes]
rs2446961	0.86[ASN][1000 genomes]
rs318069	0.94[ASN][1000 genomes]
rs318074	0.95[ASN][1000 genomes]
rs318075	0.89[ASN][1000 genomes]
rs318076	0.91[ASN][1000 genomes]
rs318077	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs318080	0.93[ASN][1000 genomes]
rs318082	0.93[ASN][1000 genomes]
rs318083	0.93[ASN][1000 genomes]
rs318085	0.93[ASN][1000 genomes]
rs318089	0.91[ASN][1000 genomes]
rs3844180	0.97[ASN][1000 genomes]
rs6451576	0.86[ASN][1000 genomes]
rs7724484	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41436200-41451800	Weak transcription	Ovary	ovary
2	chr5:41443600-41456200	Enhancers	Fetal Heart	heart
3	chr5:41445800-41450800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:41448000-41450200	Weak transcription	Right Ventricle	heart
5	chr5:41448000-41450800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr5:41448400-41449800	Weak transcription	Fetal Intestine Large	intestine
7	chr5:41448600-41453800	Weak transcription	Left Ventricle	heart
8	chr5:41449000-41449800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:41449600-41449800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr5:41449600-41451400	Enhancers	Fetal Intestine Small	intestine

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