Variant report

Variant	rs7987307
Chromosome Location	chr13:95614374-95614375
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11616336	0.86[AMR][1000 genomes]
rs11616452	0.86[AMR][1000 genomes]
rs11619067	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12856105	0.86[AMR][1000 genomes]
rs12860875	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12862417	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12871881	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34926569	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs35487217	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs35649151	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs35781706	0.83[AMR][1000 genomes]
rs36113741	0.86[AMR][1000 genomes]
rs71431487	0.83[AMR][1000 genomes]
rs71431489	0.83[AMR][1000 genomes]
rs9516499	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9516503	0.86[AMR][1000 genomes]
rs9524715	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9524718	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9524726	0.86[AMR][1000 genomes]
rs9645883	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95609600-95616200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr13:95612600-95616000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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