Variant report

Variant	rs10835883
Chromosome Location	chr11:32328565-32328566
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1022624	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1022625	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10488685	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10835879	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10835884	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10835885	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11031704	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11031714	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11031716	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11828433	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12285028	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12285041	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12361455	1.00[ASN][1000 genomes]
rs2003731	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61889170	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61889172	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61889173	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7106353	0.82[EUR][1000 genomes]
rs7116279	0.87[EUR][1000 genomes]
rs7121219	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs742994	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs742995	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs742996	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7924866	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7928458	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7944182	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32325000-32334200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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