Variant report

Variant	rs73739933
Chromosome Location	chr6:50065440-50065441
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12213027	0.81[ASN][1000 genomes]
rs1555679	1.00[ASN][1000 genomes]
rs1575590	1.00[ASN][1000 genomes]
rs57851256	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6916616	0.81[ASN][1000 genomes]
rs73739923	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73739929	1.00[EUR][1000 genomes]
rs73739930	1.00[EUR][1000 genomes]
rs73739931	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73739932	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73739934	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73739935	1.00[EUR][1000 genomes]
rs7764678	0.81[ASN][1000 genomes]
rs932741	1.00[ASN][1000 genomes]
rs9395549	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:50060000-50066000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:50064400-50066200	Enhancers	Fetal Brain Male	brain
3	chr6:50064600-50066000	Weak transcription	Fetal Intestine Large	intestine
4	chr6:50064600-50066400	Weak transcription	Fetal Brain Female	brain
5	chr6:50065000-50066200	Enhancers	Fetal Lung	lung
6	chr6:50065200-50066000	Weak transcription	Liver	Liver

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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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