Variant report

Variant	rs62545985
Chromosome Location	chr9:73422422-73422423
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs17463001	1.00[EUR][1000 genomes]
rs17463279	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17463300	0.97[EUR][1000 genomes]
rs17463328	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17463426	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17470402	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17470784	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17470826	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17554439	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17554479	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17555728	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17556102	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17556199	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35881499	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62545301	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62545305	0.92[EUR][1000 genomes]
rs62545306	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62545337	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62545982	0.90[EUR][1000 genomes]
rs62545984	1.00[EUR][1000 genomes]
rs62545989	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62545990	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62545991	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62545992	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62545993	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62545994	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62545996	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62545997	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62545998	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62545999	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62546000	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62547568	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62547569	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62547570	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62547572	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62547573	1.00[EUR][1000 genomes]
rs718445	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs718446	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893440	chr9:73225802-73434585	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	76 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73407400-73427000	Weak transcription	Aorta	Aorta
2	chr9:73411200-73437400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr9:73411800-73433400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:73418200-73444000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr9:73418200-73447400	Weak transcription	Fetal Kidney	kidney
6	chr9:73421400-73425600	Weak transcription	Fetal Brain Male	brain

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