Variant report

Variant	rs6939221
Chromosome Location	chr6:15931693-15931694
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10214915	0.80[EUR][1000 genomes]
rs10949321	0.81[EUR][1000 genomes]
rs1122664	0.80[EUR][1000 genomes]
rs1269141	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1810476	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2105356	0.91[EUR][1000 genomes]
rs4712267	0.90[EUR][1000 genomes]
rs6459428	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6932531	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs808366	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9765919	0.82[EUR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15928000-15936400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:15930800-15931800	ZNF genes & repeats	Placenta	Placenta
3	chr6:15931600-15932000	Weak transcription	Left Ventricle	heart
4	chr6:15931600-15933200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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Input of quick search could be:

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

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