Variant report

Variant	rs1928005
Chromosome Location	chr1:179523275-179523276
allele	C/G
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]
rs12021876	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12216994	0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs12216996	0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1410586	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2274624	0.86[EUR][1000 genomes]
rs3767841	0.84[AFR][1000 genomes]
rs3818587	0.86[EUR][1000 genomes]
rs60323829	0.88[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs73051834	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179522000-179523600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:179523200-179524600	Enhancers	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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