Variant report

Variant	rs2462614
Chromosome Location	chr7:13549016-13549017
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10429087	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12534739	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404937	0.91[ASN][1000 genomes]
rs1404938	0.83[ASN][1000 genomes]
rs1663	0.83[ASN][1000 genomes]
rs17280283	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2091310	0.83[ASN][1000 genomes]
rs2462613	0.83[ASN][1000 genomes]
rs2466495	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2466496	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2466498	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2692466	0.91[ASN][1000 genomes]
rs2692467	0.83[ASN][1000 genomes]
rs2692468	0.83[ASN][1000 genomes]
rs2692472	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2692479	0.91[ASN][1000 genomes]
rs2692480	0.91[ASN][1000 genomes]
rs2692481	0.91[ASN][1000 genomes]
rs2692482	0.91[ASN][1000 genomes]
rs2692483	0.91[ASN][1000 genomes]
rs2692484	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2692485	0.91[ASN][1000 genomes]
rs2692486	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2692487	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2692489	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2723394	0.91[ASN][1000 genomes]
rs2723396	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723483	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723486	0.83[ASN][1000 genomes]
rs2723487	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723488	0.91[ASN][1000 genomes]
rs62451874	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][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	nsv1019173	chr7:13063854-13585360	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv538737	chr7:13063854-13585360	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1023580	chr7:13403531-13624975	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1028163	chr7:13478678-13559505	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13547000-13549200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr7:13548000-13549400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:13548200-13549200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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