Variant report

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

rs_ID	r²[population]
rs16882798	1.00[EUR][1000 genomes]
rs1935518	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1935521	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1935524	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2179953	1.00[EUR][1000 genomes]
rs2796002	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2796004	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2840798	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2995344	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57695167	1.00[AMR][1000 genomes]
rs59148261	1.00[EUR][1000 genomes]
rs7743377	1.00[EUR][1000 genomes]
rs7770272	1.00[EUR][1000 genomes]
rs9442833	1.00[EUR][1000 genomes]
rs9442849	1.00[EUR][1000 genomes]
rs9442852	1.00[EUR][1000 genomes]
rs9442857	1.00[EUR][1000 genomes]
rs9446723	1.00[EUR][1000 genomes]
rs9446744	1.00[EUR][1000 genomes]
rs9446747	1.00[EUR][1000 genomes]
rs9446765	1.00[EUR][1000 genomes]
rs9446766	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446767	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446768	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446770	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830690	chr6:73391428-73574304	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv830691	chr6:73530978-73743648	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
3	nsv470834	chr6:73546750-73596605	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
4	nsv886155	chr6:73551937-73649330	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73509200-73572200	Weak transcription	Primary B cells from cord blood	blood
2	chr6:73563600-73571000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr6:73566000-73569800	Weak transcription	HSMM	muscle
4	chr6:73566000-73570400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:73566800-73571000	Weak transcription	Psoas Muscle	Psoas
6	chr6:73566800-73571200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:73566800-73571600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:73567800-73570600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr6:73567800-73571000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:73567800-73571600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:73567800-73571600	Weak transcription	HMEC	breast
12	chr6:73568000-73571000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:73568200-73569800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr6:73568200-73571400	Weak transcription	NH-A	brain
15	chr6:73568200-73571600	Weak transcription	NHEK	skin
16	chr6:73568400-73569600	Weak transcription	HSMMtube	muscle

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