Variant report

Variant	rs10269319
Chromosome Location	chr7:103590739-103590740
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10230291	0.89[CEU][hapmap];0.90[CHB][hapmap];0.88[YRI][hapmap];0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12666126	0.81[EUR][1000 genomes]
rs12666162	0.83[EUR][1000 genomes]
rs12666169	0.89[CEU][hapmap];0.90[CHB][hapmap];0.86[EUR][1000 genomes]
rs12666713	0.89[CEU][hapmap];0.90[CHB][hapmap];0.86[EUR][1000 genomes]
rs12666749	0.89[CEU][hapmap];0.90[CHB][hapmap];0.86[EUR][1000 genomes]
rs12671050	0.86[EUR][1000 genomes]
rs7794238	0.89[CEU][hapmap];0.90[CHB][hapmap];0.86[EUR][1000 genomes]
rs7794418	0.89[CEU][hapmap];0.90[CHB][hapmap];0.88[EUR][1000 genomes]
rs961206	0.80[CEU][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103584800-103596800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:103585400-103596000	Weak transcription	HepG2	liver
3	chr7:103590600-103597200	Weak transcription	K562	blood

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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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