Variant report

Variant	rs12347917
Chromosome Location	chr9:96184505-96184506
allele	A/G
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]
rs10115890	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10119044	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10119048	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10120391	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10121801	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10992730	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12345304	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12345623	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73651207	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73651208	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7849843	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7867699	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7868092	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96182600-96185600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:96182600-96185600	Weak transcription	Gastric	stomach
3	chr9:96184000-96184600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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