Variant report

Variant	rs73453567
Chromosome Location	chr9:72250642-72250643
allele	A/C
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]
rs10511967	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10780542	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1854704	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4744574	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7020412	0.91[EUR][1000 genomes]
rs73453565	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7849891	0.84[EUR][1000 genomes]
rs7856518	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7856629	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7874873	0.91[EUR][1000 genomes]
rs959133	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72240400-72260200	Weak transcription	Brain Anterior Caudate	brain
2	chr9:72242200-72260200	Weak transcription	Fetal Lung	lung
3	chr9:72242600-72252600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr9:72247200-72252400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr9:72247400-72264200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr9:72248200-72253200	Weak transcription	Pancreas	Pancrea
7	chr9:72248800-72252400	Weak transcription	Brain Hippocampus Middle	brain
8	chr9:72249000-72252800	Weak transcription	Fetal Kidney	kidney
9	chr9:72249200-72252800	Weak transcription	Liver	Liver
10	chr9:72249400-72252400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr9:72249800-72252400	Weak transcription	HSMM	muscle
12	chr9:72250200-72261400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr9:72250600-72250800	Enhancers	HUVEC	blood vessel

Quick Search:

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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