Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:76528266..76531083-chr1:76533694..76535257,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11585383	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11800149	0.88[AFR][1000 genomes]
rs1251464	0.81[EUR][1000 genomes]
rs1251465	0.89[ASN][1000 genomes]
rs1335740	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17097987	0.81[AFR][1000 genomes]
rs17660501	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17660531	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2043799	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs55811448	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs59469604	0.88[AFR][1000 genomes]
rs61287523	0.81[AFR][1000 genomes]
rs61771321	0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6683884	0.94[EUR][1000 genomes]
rs6692547	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72988538	0.88[AFR][1000 genomes]
rs7512384	0.85[AFR][1000 genomes]
rs7523556	0.88[AFR][1000 genomes]
rs7535776	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7536525	0.88[AFR][1000 genomes]
rs7545733	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998499	chr1:76361784-76598712	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv870968	chr1:76490234-76552475	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv947186	chr1:76512447-76530843	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1477	chr1:76515963-76534339	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv521786	chr1:76525783-76535434	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv871862	chr1:76525783-76598209	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76521800-76531000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:76526200-76531000	Weak transcription	A549	lung
3	chr1:76529800-76531600	Enhancers	Placenta Amnion	Placenta Amnion

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