Variant report

Variant	rs7911298
Chromosome Location	chr10:97765672-97765673
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1011689	0.81[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1023331	0.85[ASN][1000 genomes]
rs10748652	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10786256	0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10882710	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1556744	0.84[ASN][1000 genomes]
rs2015029	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2095591	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3748224	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4145209	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6584044	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6584045	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6584046	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7096743	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7913835	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7919099	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97765400-97777200	Weak transcription	Brain Hippocampus Middle	brain
2	chr10:97765600-97767000	Weak transcription	Aorta	Aorta

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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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