Variant report

Variant	rs12284928
Chromosome Location	chr11:102680776-102680777
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1034374	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1034375	0.92[EUR][1000 genomes]
rs11225429	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11225439	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12277638	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12289128	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3025067	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3025090	1.00[ASN][1000 genomes]
rs41380244	1.00[ASN][1000 genomes]
rs58264782	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7117506	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102678800-102690000	Weak transcription	Gastric	stomach
2	chr11:102679000-102690400	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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