Variant report

Variant	rs7864834
Chromosome Location	chr9:96185393-96185394
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10115231	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10116211	1.00[AFR][1000 genomes]
rs10121042	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10121418	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10122307	0.92[AFR][1000 genomes]
rs10125213	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10125504	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10125642	1.00[AMR][1000 genomes]
rs10992753	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12336645	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12336831	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12338407	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12339736	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12340218	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12344021	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12351051	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2150750	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28391568	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61256841	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7021294	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7034881	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7847794	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7868214	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96182600-96185600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:96182600-96185600	Weak transcription	Gastric	stomach
3	chr9:96184600-96186200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr9:96185200-96185400	Enhancers	Colon Smooth Muscle	Colon
5	chr9:96185200-96185800	Enhancers	Fetal Brain Female	brain
6	chr9:96185200-96186000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr9:96185200-96186000	Enhancers	Fetal Stomach	stomach

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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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