Variant report

Variant	rs60233772
Chromosome Location	chr9:110417741-110417742
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:110247289..110249056-chr9:110417408..110419727,2	MCF-7	breast:
2	chr9:110248485..110251289-chr9:110415972..110418067,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136826	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12001098	0.83[EUR][1000 genomes]
rs12339806	0.93[EUR][1000 genomes]
rs12339850	0.91[EUR][1000 genomes]
rs12347544	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12347609	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12347622	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12350134	0.91[EUR][1000 genomes]
rs12352414	0.92[EUR][1000 genomes]
rs2417802	0.86[AMR][1000 genomes]
rs28379887	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28410234	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28501144	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28545042	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28558750	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28718553	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28756961	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41368853	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55732410	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57223814	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58725849	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7341759	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7341900	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73653618	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7868525	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7875152	0.83[EUR][1000 genomes]
rs940291	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831683	chr9:110275212-110461288	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv893700	chr9:110365337-110451516	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110413000-110437000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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