Variant report

Variant	rs11977330
Chromosome Location	chr7:52790030-52790031
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:52785933..52787584-chr7:52789855..52792602,2	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10215086	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11238229	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11238230	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11974892	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11980050	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1230547	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1230549	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12668035	0.99[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1528997	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1528998	0.96[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1528999	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1627324	0.81[EUR][1000 genomes]
rs1649716	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1649721	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1649727	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1649733	0.80[ASN][1000 genomes]
rs1729831	0.81[EUR][1000 genomes]
rs1729857	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1978593	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs28469789	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs35116687	0.88[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs35610141	0.87[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs4418303	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs60716577	0.81[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6958886	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7777290	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7806644	0.80[ASN][1000 genomes]
rs9690428	0.87[AFR][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	nsv888026	chr7:52588348-53013671	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv888027	chr7:52588348-53190508	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1019722	chr7:52767403-52800721	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv538842	chr7:52767403-52800721	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:52785600-52804400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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