Variant report

Variant	rs17146002
Chromosome Location	chr11:83441437-83441438
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10501547	0.92[AMR][1000 genomes]
rs11233735	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12797204	0.85[YRI][hapmap];0.82[AFR][1000 genomes]
rs12807660	0.85[AFR][1000 genomes]
rs17146000	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17146016	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35248605	0.95[AFR][1000 genomes]
rs59776077	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61440361	0.92[AMR][1000 genomes]
rs7119373	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83439600-83443600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr11:83439800-83448000	Weak transcription	Brain Anterior Caudate	brain
3	chr11:83440000-83446600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr11:83440000-83446800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr11:83440800-83446800	Weak transcription	Brain Angular Gyrus	brain
6	chr11:83440800-83447200	Weak transcription	Brain Hippocampus Middle	brain

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

what's new

Quick links