Variant report

Variant	rs72741452
Chromosome Location	chr9:103944122-103944123
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F4	chr9:103944118-103944374	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
ENSG00000148123	TF binding region

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10512278	0.83[AMR][1000 genomes]
rs10989419	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10989421	0.95[ASN][1000 genomes]
rs12341807	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12344899	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12344900	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12376727	0.95[ASN][1000 genomes]
rs1431472	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17762396	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17829436	0.83[AMR][1000 genomes]
rs17829926	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1987400	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs41274975	0.83[AMR][1000 genomes]
rs4278208	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4342669	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4743445	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4743446	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4743449	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4743450	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55672230	0.83[AMR][1000 genomes]
rs55903434	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs56156225	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs57097151	0.82[EUR][1000 genomes]
rs57409431	0.83[AMR][1000 genomes]
rs58088765	0.83[AMR][1000 genomes]
rs61489062	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72741437	0.83[AMR][1000 genomes]
rs72741438	0.83[AMR][1000 genomes]
rs72741439	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72741445	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72741449	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7852006	0.82[AMR][1000 genomes];0.80[EUR][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	nsv831671	chr9:103858107-104020816	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv948791	chr9:103893030-103964650	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	5 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	chr9:103937400-103946000	Weak transcription	HepG2	liver

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