Variant report

Variant	rs1351117
Chromosome Location	chr9:96179785-96179786
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10821124	0.93[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs10992729	0.95[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12379660	0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs13287066	0.95[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs2151713	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4481672	0.88[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs7022679	0.93[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs7870079	0.83[AFR][1000 genomes];0.94[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96178200-96181000	Enhancers	Placenta	Placenta
2	chr9:96179600-96182000	Weak transcription	H1 BMP4 Derived Trophoblast 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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