Variant report

Variant	rs12297507
Chromosome Location	chr12:118168947-118168948
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10466935	1.00[EUR][1000 genomes]
rs11068642	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11068644	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11068646	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11068647	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11068649	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11068656	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11068691	1.00[EUR][1000 genomes]
rs11068692	1.00[EUR][1000 genomes]
rs11068693	1.00[EUR][1000 genomes]
rs12231482	1.00[EUR][1000 genomes]
rs12297629	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12321247	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16951457	1.00[EUR][1000 genomes]
rs56322070	1.00[EUR][1000 genomes]
rs6490158	1.00[EUR][1000 genomes]
rs6490159	1.00[EUR][1000 genomes]
rs9651900	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118159400-118172400	Weak transcription	Pancreas	Pancrea
2	chr12:118168800-118169400	Weak transcription	iPS DF 19.11 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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