Variant report

Variant	rs68093214
Chromosome Location	chr3:70657785-70657786
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10511000	1.00[ASN][1000 genomes]
rs13066991	0.89[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13070884	1.00[ASN][1000 genomes]
rs13094712	1.00[ASN][1000 genomes]
rs1491602	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1565551	1.00[ASN][1000 genomes]
rs35071663	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35751372	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35807064	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4491862	1.00[ASN][1000 genomes]
rs6786654	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs957343	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs957344	0.81[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	chr3:70645400-70663400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:70655000-70663400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:70657600-70658200	Active TSS	Pancreatic Islets	Pancreatic Islet

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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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