Variant report

Variant	rs790358
Chromosome Location	chr11:83624269-83624270
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs2625521	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2675717	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2852735	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2852736	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83607200-83628800	Weak transcription	Brain Angular Gyrus	brain
2	chr11:83608400-83634600	Weak transcription	Brain Hippocampus Middle	brain
3	chr11:83608800-83629400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:83618200-83641200	Weak transcription	Brain Anterior Caudate	brain
5	chr11:83621000-83629400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr11:83623200-83635800	Weak transcription	Brain Substantia Nigra	brain
7	chr11:83623600-83626000	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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