Variant report

Variant	rs73906316
Chromosome Location	chr21:39892356-39892357
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17230638	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17230645	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2836421	0.83[ASN][1000 genomes]
rs2836468	0.92[EUR][1000 genomes]
rs2836470	0.92[EUR][1000 genomes]
rs3787911	0.92[EUR][1000 genomes]
rs59887250	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7283796	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73906313	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39891400-39895400	Weak transcription	Aorta	Aorta
2	chr21:39891800-39892600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr21:39892000-39896000	Enhancers	HepG2	liver

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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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