Variant report

Variant	rs2153910
Chromosome Location	chr6:15973868-15973869
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12660370	0.87[ASN][1000 genomes]
rs12665492	0.90[ASN][1000 genomes]
rs4712270	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4716018	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55968425	0.89[EUR][1000 genomes]
rs67757263	0.89[ASN][1000 genomes]
rs6925493	0.89[ASN][1000 genomes]
rs9383095	0.89[EUR][1000 genomes]
rs9383099	0.89[ASN][1000 genomes]
rs9396620	0.89[EUR][1000 genomes]
rs9396624	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9476999	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9477000	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15970600-15980800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:15973600-15974800	Weak transcription	Aorta	Aorta

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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