Variant report

Variant	rs9860621
Chromosome Location	chr3:34615743-34615744
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11129598	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13074645	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1520641	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1520644	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2167041	0.83[EUR][1000 genomes]
rs2167042	0.83[EUR][1000 genomes]
rs2336653	0.81[EUR][1000 genomes]
rs4678695	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6798617	0.93[EUR][1000 genomes]
rs7614078	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7629903	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34615400-34616600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:34615600-34617400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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