Variant report

Variant	rs11087178
Chromosome Location	chr20:16605627-16605628
allele	C/G
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]
rs17675492	1.00[JPT][hapmap]
rs6075087	1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs6080319	1.00[AFR][1000 genomes]
rs6080323	1.00[AFR][1000 genomes]
rs6080331	1.00[AFR][1000 genomes]
rs6080335	1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs6080337	1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs6080342	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs73106829	1.00[AFR][1000 genomes]
rs7352087	1.00[AFR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:16603400-16607000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr20:16604800-16606200	Weak transcription	Placenta	Placenta
3	chr20:16605400-16606600	Enhancers	Fetal Stomach	stomach
4	chr20:16605600-16605800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr20:16605600-16606200	Enhancers	Fetal Lung	lung
6	chr20:16605600-16628800	Weak transcription	H1 BMP4 Derived Mesendoderm 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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