Variant report

Variant	rs6892949
Chromosome Location	chr5:16374727-16374728
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10520839	1.00[ASN][1000 genomes]
rs12187808	1.00[ASN][1000 genomes]
rs12187814	1.00[ASN][1000 genomes]
rs12187846	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12188926	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868550	1.00[ASN][1000 genomes]
rs16868571	1.00[ASN][1000 genomes]
rs16868576	1.00[ASN][1000 genomes]
rs60212641	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6878840	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73753326	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9686174	1.00[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16372800-16376800	Weak transcription	Pancreas	Pancrea
2	chr5:16373400-16375600	Weak transcription	Psoas Muscle	Psoas
3	chr5:16373800-16375400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:16374400-16377200	Weak transcription	Fetal Heart	heart

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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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